-
1
-
-
0000016355
-
The porphyrias
-
Scriver CR, Beaudet AL, Sly WS, Valle D (eds). 7th ed. New York, McGraw Hill
-
Kappas A, Sassa S, Galbraith RA, et al The porphyrias. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds). The metabolic basis of inherited diseases. Vol. 2. 7th ed. New York, McGraw Hill, 1995, pp 2103-2159
-
(1995)
The Metabolic Basis of Inherited Diseases
, vol.2
, pp. 2103-2159
-
-
Kappas, A.1
Sassa, S.2
Galbraith, R.A.3
-
2
-
-
6844240444
-
Clinical diagnosis, prevention and management of the hepatic porphyrias
-
Schmid R, Bianchi L, Blum HE, et al. (eds). Kluwer Academic Publishers, Dordrecht/Boston/London
-
Hift RG, Meissner PN, Kirsch R. Clinical diagnosis, prevention and management of the hepatic porphyrias. In: Schmid R, Bianchi L, Blum HE, et al. (eds). Acute and chronic liver diseases Molecular biology and clinics. Klu wer Academic Publishers, Dordrecht/Boston/London, 1996, pp 201-215
-
(1996)
Acute and Chronic Liver Diseases Molecular Biology and Clinics
, pp. 201-215
-
-
Hift, R.G.1
Meissner, P.N.2
Kirsch, R.3
-
3
-
-
0031940457
-
Acute porphyna: Treatment with heme
-
PagesTK
-
Tenhunen R, Mustajoki P. Acute porphyna: treatment with heme. Sem Liv Dis 18:(PagesTK), 1998
-
(1998)
Sem Liv Dis
, vol.18
-
-
Tenhunen, R.1
Mustajoki, P.2
-
4
-
-
0030069657
-
Porphobilinogen deaminase deficiency in mice causes a neuropathy resembling that of human hepatic porphyna
-
Lindberg RLP, Porcher C, Grandchamp B, et al. Porphobilinogen deaminase deficiency in mice causes a neuropathy resembling that of human hepatic porphyna. Nature Genet 1996;12: 195-199
-
(1996)
Nature Genet
, vol.12
, pp. 195-199
-
-
Lindberg, R.L.P.1
Porcher, C.2
Grandchamp, B.3
-
5
-
-
0021188334
-
Molecular cloning of a cDNA sequence complementary to porphobilinogen deaminase mRNA from rat
-
Grandchamp B, Romeo PH, Dubart A, et al. Molecular cloning of a cDNA sequence complementary to porphobilinogen deaminase mRNA from rat. Proc Natl Acad Sci USA 1984;81:5036-5040
-
(1984)
Proc Natl Acad Sci USA
, vol.81
, pp. 5036-5040
-
-
Grandchamp, B.1
Romeo, P.H.2
Dubart, A.3
-
6
-
-
0023046949
-
Molecular cloning and complete primary sequence of human erythrocyte porphobilinogen deaminase
-
Raich N, Romeo PH, Dubart A, et al. Molecular cloning and complete primary sequence of human erythrocyte porphobilinogen deaminase. Nucleic Acids Res 1986;14:5955-5968
-
(1986)
Nucleic Acids Res
, vol.14
, pp. 5955-5968
-
-
Raich, N.1
Romeo, P.H.2
Dubart, A.3
-
7
-
-
0023141499
-
Tissue-specific expression of porphobilinogen deaminase. Two isoenzymes from a single gene
-
Grandchamp B, de Verneuil H, Beaumont C, et al Tissue-specific expression of porphobilinogen deaminase. Two isoenzymes from a single gene. Eur J Biochem 1987;162:105-110
-
(1987)
Eur J Biochem
, vol.162
, pp. 105-110
-
-
Grandchamp, B.1
De Verneuil, H.2
Beaumont, C.3
-
8
-
-
0027946035
-
The three-dimensional structures of mutants of porphobilinogen deaminase: Toward an understanding of the structural basis of acute intermittent porphyria
-
Brownlie PD, Lambert R, Louie GV, et al. The three-dimensional structures of mutants of porphobilinogen deaminase: toward an understanding of the structural basis of acute intermittent porphyria. Protein Sci 1994;3:1644-1650
-
(1994)
Protein Sci
, vol.3
, pp. 1644-1650
-
-
Brownlie, P.D.1
Lambert, R.2
Louie, G.V.3
-
9
-
-
0023713201
-
Alternative transcription and splicing of the human porphobilinogen deaminase gene result either in tissue-specific or in housekeeping expression
-
Chretien S, Dubart A, Beaupain D, et al. Alternative transcription and splicing of the human porphobilinogen deaminase gene result either in tissue-specific or in housekeeping expression. Proc Natl Acad Sci USA 1988;85:6-10
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 6-10
-
-
Chretien, S.1
Dubart, A.2
Beaupain, D.3
-
10
-
-
0025895524
-
Assignment of human PBGD to 11q24.1 → 11q24.2 by in situ hybridization and gene dosage studies
-
Namba M, Narahara K, Tsuji K, et al. Assignment of human PBGD to 11q24.1 → 11q24.2 by in situ hybridization and gene dosage studies. Cyto Cell Genet 1991;67:105-108
-
(1991)
Cyto Cell Genet
, vol.67
, pp. 105-108
-
-
Namba, M.1
Narahara, K.2
Tsuji, K.3
-
11
-
-
0027409758
-
Hydroxymethylbilane synthase: Complete genomic sequence and amplifiable polymorphisms in the human gene
-
Yoo HW, Warner CA, Chen CH, et al Hydroxymethylbilane synthase: complete genomic sequence and amplifiable polymorphisms in the human gene. Genomics 1993;15:21-29
-
(1993)
Genomics
, vol.15
, pp. 21-29
-
-
Yoo, H.W.1
Warner, C.A.2
Chen, C.H.3
-
12
-
-
0024534370
-
Two tissue-specific factors bind the erythroid promoter of the human porphobilinogen deaminase gene
-
Mignotte V, Wall L, deBoer E, et al. Two tissue-specific factors bind the erythroid promoter of the human porphobilinogen deaminase gene. Nucleic Acids Res 1989;17:37-54
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 37-54
-
-
Mignotte, V.1
Wall, L.2
DeBoer, E.3
-
13
-
-
0024541345
-
Tissue-specific splicing mutation in acute intermittent porphyria
-
Grandchamp B, Picat C, Mignotte V, et al. Tissue-specific splicing mutation in acute intermittent porphyria. Proc Natl Acad Sci USA 1989;86:661-664
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 661-664
-
-
Grandchamp, B.1
Picat, C.2
Mignotte, V.3
-
14
-
-
0024424094
-
Molecular analysis of acute intermittent porphyria in a Finnish family with normal erythrocyte porphobilinogen deaminase
-
Grandchamp B, Picat C, Kauppinen R, et al. Molecular analysis of acute intermittent porphyria in a Finnish family with normal erythrocyte porphobilinogen deaminase. Eur J Clin Invest 1989; 19:415-418
-
(1989)
Eur J Clin Invest
, vol.19
, pp. 415-418
-
-
Grandchamp, B.1
Picat, C.2
Kauppinen, R.3
-
15
-
-
0028113944
-
Acute intermittent porphyria: Identification and expression of exonic mutations in the hydroxymethylbilane synthase gene. An initiation codon missense mutation in the housekeeping transcript causes "variant acute intermittent porphyria" with normal expression of the erythroid-specific enzyme
-
Chen CH, Astrin KH, Lee G, et al. Acute intermittent porphyria: identification and expression of exonic mutations in the hydroxymethylbilane synthase gene. An initiation codon missense mutation in the housekeeping transcript causes "variant acute intermittent porphyria" with normal expression of the erythroid-specific enzyme. J Clin Invest 1994;94:1927-1937
-
(1994)
J Clin Invest
, vol.94
, pp. 1927-1937
-
-
Chen, C.H.1
Astrin, K.H.2
Lee, G.3
-
16
-
-
6844257796
-
Detection of three mutations in four patients with acute intermittent porphyria
-
Ong PML, Lanyon WG, Hilt R, et al. Detection of three mutations in four patients with acute intermittent porphyria. Scand J Clin Lab 55 (suppl) 1995;223:132A
-
(1995)
Scand J Clin Lab 55 (Suppl)
, vol.223
-
-
Ong, P.M.L.1
Lanyon, W.G.2
Hilt, R.3
-
17
-
-
0028945782
-
Acute intermittent porphyria in Finland: 19 mutations in the porphobilinogen deaminase gene
-
Kauppinen R, Mustajoki S, Pihlaja H, et al. Acute intermittent porphyria in Finland: 19 mutations in the porphobilinogen deaminase gene. Hum Mol Genet 1995;4235:215-222
-
(1995)
Hum Mol Genet
, vol.4235
, pp. 215-222
-
-
Kauppinen, R.1
Mustajoki, S.2
Pihlaja, H.3
-
18
-
-
0027181454
-
Acute intermittent porphyria caused by an arginine to histidine substitution (R26H) in the cofactor-binding cleft of porphobilinogen deaminase
-
Llewellyn DH, Whatley S, Elder GH. Acute intermittent porphyria caused by an arginine to histidine substitution (R26H) in the cofactor-binding cleft of porphobilinogen deaminase. Hum Molec Genet 1993;2:1315-1316
-
(1993)
Hum Molec Genet
, vol.2
, pp. 1315-1316
-
-
Llewellyn, D.H.1
Whatley, S.2
Elder, G.H.3
-
19
-
-
6844251844
-
Molecular epidemiology and diagnosis of acute intermittent porphyria
-
in press
-
Puy H, Deybach J-C, Lamoril J, et al. Molecular epidemiology and diagnosis of acute intermittent porphyria. Amer J Hum Genet 1997, in press
-
(1997)
Amer J Hum Genet
-
-
Puy, H.1
Deybach, J.-C.2
Lamoril, J.3
-
20
-
-
6844254799
-
Mutation spectrum of the porphobilinogen deaminase gene in the Finnish patients with acute intermittent porphyria
-
Mustajoki S, Kauppinen R, Peltonen L, et al. Mutation spectrum of the porphobilinogen deaminase gene in the Finnish patients with acute intermittent porphyria. Scand J Clin Lab 55 (suppl) 1995;223:25A
-
(1995)
Scand J Clin Lab 55 (Suppl)
, vol.223
-
-
Mustajoki, S.1
Kauppinen, R.2
Peltonen, L.3
-
21
-
-
0028858113
-
Four mutations in the PBGD gene in patients with AIP
-
Lundin G, Hashemi J, Floderus Y, et al. Four mutations in the PBGD gene in patients with AIP. J Med Genet 1995;32:979-981
-
(1995)
J Med Genet
, vol.32
, pp. 979-981
-
-
Lundin, G.1
Hashemi, J.2
Floderus, Y.3
-
22
-
-
0028032023
-
Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresis
-
Gu XF, de Rooij F, Voortman G, et al. Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresis. Hum Genet 1994;93:47-52
-
(1994)
Hum Genet
, vol.93
, pp. 47-52
-
-
Gu, X.F.1
De Rooij, F.2
Voortman, G.3
-
23
-
-
0026808849
-
Detection of seven point mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria, by direct sequencing of in vitro amplified cDNA
-
Mgone CS, Lanyon WG, Moore MR, et al Detection of seven point mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria, by direct sequencing of in vitro amplified cDNA. Hum Genet 1992;90:12-16
-
(1992)
Hum Genet
, vol.90
, pp. 12-16
-
-
Mgone, C.S.1
Lanyon, W.G.2
Moore, M.R.3
-
24
-
-
0029985268
-
Detection of four novel mutations in the porphobilinogen deaminase gene in French Caucasian patients with acute intermittent porphyria
-
Puy H, Deybach JC, Lamoril J, et al. Detection of four novel mutations in the porphobilinogen deaminase gene in French Caucasian patients with acute intermittent porphyria. Hum Hered 1996;46:177-178
-
(1996)
Hum Hered
, vol.46
, pp. 177-178
-
-
Puy, H.1
Deybach, J.C.2
Lamoril, J.3
-
25
-
-
0029037656
-
Heteroduplex analysis detects frameshift and point mutations in patients with acute intermittent porphyria
-
Schreiber WE, Fong F, Nassar BA, et al. Heteroduplex analysis detects frameshift and point mutations in patients with acute intermittent porphyria Hum Genet 1995;96:161-166
-
(1995)
Hum Genet
, vol.96
, pp. 161-166
-
-
Schreiber, W.E.1
Fong, F.2
Nassar, B.A.3
-
26
-
-
6844240443
-
Frequency and distribution of mutations in the gene of porphobilinogen deaminase in Dutch acute intermittent porphyria patients
-
de Rooij FWM, Voortman G, de Baar E, et al. Frequency and distribution of mutations in the gene of porphobilinogen deaminase in Dutch acute intermittent porphyria patients. Scand J Clin Lab 55 (suppl) 1995;223:24A
-
(1995)
Scand J Clin Lab 55 (Suppl)
, vol.223
-
-
De Rooij, F.W.M.1
Voortman, G.2
De Baar, E.3
-
27
-
-
0027373331
-
Two novel mutations of the porphobilinogen deaminase gene in acute intermittent porphyria
-
Gu XF, de Rooij F, de Baar E, et al. Two novel mutations of the porphobilinogen deaminase gene in acute intermittent porphyria Hum Mol Genet 1993;2:1735-1736
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1735-1736
-
-
Gu, X.F.1
De Rooij, F.2
De Baar, E.3
-
28
-
-
0028211734
-
Frameshift mutations in exons 9 and 10 of the porphobilinogen deaminase gene produce a crossreacting immunological material (CRIM)-negative form of acute intermittent porphyria
-
Schreiber WE, Fong F, Jamani A. Frameshift mutations in exons 9 and 10 of the porphobilinogen deaminase gene produce a crossreacting immunological material (CRIM)-negative form of acute intermittent porphyria. Hum Genet 1994;93:552-556
-
(1994)
Hum Genet
, vol.93
, pp. 552-556
-
-
Schreiber, W.E.1
Fong, F.2
Jamani, A.3
-
29
-
-
0025105093
-
Haplotyping of the human porphobilinogen deaminase gene in acute intermittent porphyria by polymerase chain reaction
-
Lee JS, Lindsten J, Anvret M. Haplotyping of the human porphobilinogen deaminase gene in acute intermittent porphyria by polymerase chain reaction. Hum Genet 1990;84:241-243
-
(1990)
Hum Genet
, vol.84
, pp. 241-243
-
-
Lee, J.S.1
Lindsten, J.2
Anvret, M.3
-
30
-
-
0028316669
-
Identification of five novel mutations in the porphobilinogen deaminase gene
-
Mgone CS, Lanyon WG, Moore MR, et al Identification of five novel mutations in the porphobilinogen deaminase gene. Hum Mol Genet 1994;3 809-811
-
(1994)
Hum Mol Genet
, vol.3
, pp. 809-811
-
-
Mgone, C.S.1
Lanyon, W.G.2
Moore, M.R.3
-
31
-
-
0026327963
-
Molecular heterogeneity of acute intermittent porphyria: Identification of four additional mutations resulting in the CRIM-negative subtype of the disease
-
Delfau MH, Picat C, de Rooij F, et al. Molecular heterogeneity of acute intermittent porphyria: identification of four additional mutations resulting in the CRIM-negative subtype of the disease Am J Hum Genet 1991;49:421-428
-
(1991)
Am J Hum Genet
, vol.49
, pp. 421-428
-
-
Delfau, M.H.1
Picat, C.2
De Rooij, F.3
-
32
-
-
0025034507
-
Acute intermittent porphyria caused by a C - T mutation that produces a stop codon in the porphobilinogen deaminase gene
-
Scobie GA, Llewellyn DH, Urquhart AJ, et al. Acute intermittent porphyria caused by a C - T mutation that produces a stop codon in the porphobilinogen deaminase gene. Hum Genet 1990;85: 631-634
-
(1990)
Hum Genet
, vol.85
, pp. 631-634
-
-
Scobie, G.A.1
Llewellyn, D.H.2
Urquhart, A.J.3
-
33
-
-
6844235949
-
Characterization of mutations in the human porphobilinogen deaminase gene
-
Lundin G, Lee, JS, Persson B, et al. Characterization of mutations in the human porphobilinogen deaminase gene. Nether J Med 1993;42:A28
-
(1993)
Nether J Med
, vol.42
-
-
Lundin, G.1
Lee, J.S.2
Persson, B.3
-
34
-
-
0026712533
-
High frequency of mutations in exon 10 of the porphobilinogen deaminase gene in patients with a CRIM-positive subtype of acute intermittent porphyria
-
Gu XF, de Rooij F, Voortman G, et al. High frequency of mutations in exon 10 of the porphobilinogen deaminase gene in patients with a CRIM-positive subtype of acute intermittent porphyria. Am J Hum Genet 1992;51:660-665
-
(1992)
Am J Hum Genet
, vol.51
, pp. 660-665
-
-
Gu, X.F.1
De Rooij, F.2
Voortman, G.3
-
35
-
-
0025147496
-
Two different point G to A mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyria
-
Delfau MH, Picat C, de Rooij FW, et al. Two different point G to A mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyria. J Clin Invest 1990;86:1511-1516
-
(1990)
J Clin Invest
, vol.86
, pp. 1511-1516
-
-
Delfau, M.H.1
Picat, C.2
De Rooij, F.W.3
-
36
-
-
0025900587
-
Genetic heterogeneity of the porphobilinogen deaminase gene in Swedish families with acute intermittent porphyria
-
Lee JS, Lundin G, Lannfelt L, et al Genetic heterogeneity of the porphobilinogen deaminase gene in Swedish families with acute intermittent porphyria. Hum Genet 1991;87:484-488
-
(1991)
Hum Genet
, vol.87
, pp. 484-488
-
-
Lee, J.S.1
Lundin, G.2
Lannfelt, L.3
-
37
-
-
0025888932
-
Identification of the most common mutation within the porphobilinogen deaminase gene in Swedish patients with acute intermittent porphyria
-
Lee JS, Anvret M. Identification of the most common mutation within the porphobilinogen deaminase gene in Swedish patients with acute intermittent porphyria. Proc Natl Acad Sci USA 1991;88:10912-10915
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 10912-10915
-
-
Lee, J.S.1
Anvret, M.2
-
38
-
-
0028055199
-
Two new mutations in the porphobilinogen deaminase gene and a screening method using PCR amplification of specific alleles
-
Lundin G, Wedell A, Thunell S, et al. Two new mutations in the porphobilinogen deaminase gene and a screening method using PCR amplification of specific alleles. Hum Genet 1994;93: 59-62
-
(1994)
Hum Genet
, vol.93
, pp. 59-62
-
-
Lundin, G.1
Wedell, A.2
Thunell, S.3
-
39
-
-
0024326187
-
A point mutation G - A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria
-
Grandchamp B, Picat C, de Rooij F, et al. A point mutation G - A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria. Nucleic Acids Res 1989;17:6637-6649
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 6637-6649
-
-
Grandchamp, B.1
Picat, C.2
De Rooij, F.3
-
40
-
-
6844260756
-
Splice-defective mutations of the porphobilinogen deaminase gene responsible for acute intermittent porphyria
-
Llewellyn DH, Scobie GA, Urquhart AJ, et al. Splice-defective mutations of the porphobilinogen deaminase gene responsible for acute intermittent porphyria. Nether J Med 1993;42:A31
-
(1993)
Nether J Med
, vol.42
-
-
Llewellyn, D.H.1
Scobie, G.A.2
Urquhart, A.J.3
-
41
-
-
0027381060
-
Detection of a high mutation frequency in exon 12 of the porphobilinogen deaminase gene in patients with acute intermittent porphyria
-
Mgone CS, Lanyon WG, Moore MR, et al. Detection of a high mutation frequency in exon 12 of the porphobilinogen deaminase gene in patients with acute intermittent porphyria Hum Genet 1993;92:619-622
-
(1993)
Hum Genet
, vol.92
, pp. 619-622
-
-
Mgone, C.S.1
Lanyon, W.G.2
Moore, M.R.3
-
42
-
-
0029873603
-
Detection of four mutations in six unrelated South African patients with acute intermittent porphyria
-
Ong PM, Lanyon WG, Hift RJ,. et al. Detection of four mutations in six unrelated South African patients with acute intermittent porphyria. Mol Cell Probes 1996;10:57-61
-
(1996)
Mol Cell Probes
, vol.10
, pp. 57-61
-
-
Ong, P.M.1
Lanyon, W.G.2
Hift, R.J.3
-
43
-
-
0027430090
-
Acute intermittent porphyria caused by a G to C mutation in exon 12 of the porphobilinogen deaminase gene that results in exon skipping
-
Daimon M, Yamatani K, Igarashi M, et al. Acute intermittent porphyria caused by a G to C mutation in exon 12 of the porphobilinogen deaminase gene that results in exon skipping. Hum Genet 1993;92:549-553
-
(1993)
Hum Genet
, vol.92
, pp. 549-553
-
-
Daimon, M.1
Yamatani, K.2
Igarashi, M.3
-
44
-
-
0029065492
-
Acute intermittent porphyria in a native North American family. Biochemical and molecular analysis
-
Schreiber WE, Jamani A, Armstrong JG. Acute intermittent porphyria in a native North American family. Biochemical and molecular analysis. Am J Clin Pathol 1995;103:730-734
-
(1995)
Am J Clin Pathol
, vol.103
, pp. 730-734
-
-
Schreiber, W.E.1
Jamani, A.2
Armstrong, J.G.3
-
45
-
-
0029671327
-
R325X mutation in exon 15 of the hydroxymethylbilane synthase gene identified in two Danish families with acute intermittent porphyria
-
Petersen NE, Nissen H, Hansen TS, et al. R325X mutation in exon 15 of the hydroxymethylbilane synthase gene identified in two Danish families with acute intermittent porphyria. Clin Chem 1996;42:106-107
-
(1996)
Clin Chem
, vol.42
, pp. 106-107
-
-
Petersen, N.E.1
Nissen, H.2
Hansen, T.S.3
-
46
-
-
0028209472
-
Acute intermittent porphyria caused by a single base insertion of C in exon 15 of the porphobilinogen deaminase gene that results in a frame shift and premature stopping of translation
-
Daimon M, Yamatani K, Igarashi M, et al Acute intermittent porphyria caused by a single base insertion of C in exon 15 of the porphobilinogen deaminase gene that results in a frame shift and premature stopping of translation. Hum Genet 1994;93:533-537
-
(1994)
Hum Genet
, vol.93
, pp. 533-537
-
-
Daimon, M.1
Yamatani, K.2
Igarashi, M.3
-
47
-
-
0029097740
-
De-novo mutation and sporadic presentation of acute intermittent porphyria
-
Whatley SD, Roberts AG, Elder GH. De-novo mutation and sporadic presentation of acute intermittent porphyria. Lancet 1995; 346:1007-1008
-
(1995)
Lancet
, vol.346
, pp. 1007-1008
-
-
Whatley, S.D.1
Roberts, A.G.2
Elder, G.H.3
-
48
-
-
0026682570
-
Frequency of low erythrocyte porphobilinogen deaminase activity in Finland
-
Mustajoki P, Kauppinen R, Lannfelt L, et al. Frequency of low erythrocyte porphobilinogen deaminase activity in Finland. J Intern Med 1992;231:389-395
-
(1992)
J Intern Med
, vol.231
, pp. 389-395
-
-
Mustajoki, P.1
Kauppinen, R.2
Lannfelt, L.3
-
49
-
-
0030799468
-
Acute intermittent porphyria prevalence of mutations in the porphobilinogen deaminase gene in blood donors in France
-
Nordmann Y, Puy H, Da Silva V, et al. Acute intermittent porphyria prevalence of mutations in the porphobilinogen deaminase gene in blood donors in France. J Intern Med 1997;242: 213-217
-
(1997)
J Intern Med
, vol.242
, pp. 213-217
-
-
Nordmann, Y.1
Puy, H.2
Da Silva, V.3
|