-
1
-
-
0025854490
-
Importance of maternal history of non-insulin dependent diabetic patients
-
Alcolado JC, Alcolado R: Importance of maternal history of non-insulin dependent diabetic patients Br Med J 302: 1178-1180, 1991
-
(1991)
Br Med J
, vol.302
, pp. 1178-1180
-
-
Alcolado, J.C.1
Alcolado, R.2
-
2
-
-
0027195153
-
Japanese case of diabetes mellitus and deafness with mutation in mitochondrial tRNALeu(-UUR) gene
-
Awata T, Matsumoto T, Iwamoto Y, Matsuda A, Kuzuya T, Saito T: Japanese case of diabetes mellitus and deafness with mutation in mitochondrial tRNALeu(-UUR) gene. Lancet 341: 1291-1292, 1993
-
(1993)
Lancet
, vol.341
, pp. 1291-1292
-
-
Awata, T.1
Matsumoto, T.2
Iwamoto, Y.3
Matsuda, A.4
Kuzuya, T.5
Saito, T.6
-
3
-
-
0026849690
-
Maternally transmitted diabetes and deafness associated with a 10.4 kb deletion
-
Ballinger SW, Shoffner JM, Hedaya EV, Trounce I, Polak MA, Koontz DA, Wallace DC: Maternally transmitted diabetes and deafness associated with a 10.4 kb deletion. Nature Gen. 1: 11-15, 1992
-
(1992)
Nature Gen.
, vol.1
, pp. 11-15
-
-
Ballinger, S.W.1
Shoffner, J.M.2
Hedaya, E.V.3
Trounce, I.4
Polak, M.A.5
Koontz, D.A.6
Wallace, D.C.7
-
4
-
-
0026032055
-
Gene for non-insulin dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymor- Phism on human chromosome 20q
-
Bell GI, Xiang K, Newman MV, Wu S, Wright LG, Fajans SS, Spielman RS, Cox NJ: Gene for non-insulin dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymor- phism on human chromosome 20q. Proc Natl Acad Sci USA 88: 1484-1488, 1991
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 1484-1488
-
-
Bell, G.I.1
Xiang, K.2
Newman, M.V.3
Wu, S.4
Wright, L.G.5
Fajans, S.S.6
Spielman, R.S.7
Cox, N.J.8
-
5
-
-
0027933734
-
A genome-wide search for human type 1 diabetes susceptibility genes
-
Davies JL, Kawagushi Y, Bennett ST, Copeman JB, Cordell HJ, Pritchard LE, Reed PW, Gough SCL, Jenkins SC, Palmer SM, Balfour KM, Rowe BR, Farall M, Barnett AH, Bain SC, Todd JA: A genome-wide search for human type 1 diabetes susceptibility genes. Nature 371: 130-136, 1994
-
(1994)
Nature
, vol.371
, pp. 130-136
-
-
Davies, J.L.1
Kawagushi, Y.2
Bennett, S.T.3
Copeman, J.B.4
Cordell, H.J.5
Pritchard, L.E.6
Reed, P.W.7
Gough, S.C.L.8
Jenkins, S.C.9
Palmer, S.M.10
Balfour, K.M.11
Rowe, B.R.12
Farall, M.13
Barnett, A.H.14
Bain, S.C.15
Todd, J.A.16
-
6
-
-
0016812904
-
On possible genetic and epigenetic modes of diabetes transmission
-
Dörner G, Mohnike A, Steindel E: On possible genetic and epigenetic modes of diabetes transmission. Endokrinologie 66: 225-229, 1975
-
(1975)
Endokrinologie
, vol.66
, pp. 225-229
-
-
Dörner, G.1
Mohnike, A.2
Steindel, E.3
-
7
-
-
0026463740
-
Does the mitochondrial DNA play a role in the pathogenesis of diabetes?
-
Gerbitz, KD: Does the mitochondrial DNA play a role in the pathogenesis of diabetes? Diabetologia 35: 1181-1186, 1992
-
(1992)
Diabetologia
, vol.35
, pp. 1181-1186
-
-
Gerbitz, K.D.1
-
8
-
-
0000204255
-
Maternal inheritance of human mitochondrial DNA
-
Giles RE, Blanc H, Cann HM, Wallace DC: Maternal inheritance of human mitochondrial DNA. Proc Natl Acad Sci USA 77: 6715-6719, 1980
-
(1980)
Proc Natl Acad Sci USA
, vol.77
, pp. 6715-6719
-
-
Giles, R.E.1
Blanc, H.2
Cann, H.M.3
Wallace, D.C.4
-
9
-
-
0025666322
-
A mutation in the tRNA-Leu (UUR) gene associated with the Melas subgroup of mitochondrial encephalomyopathies
-
Goto Y, Nonaka I, Horai S: A mutation in the tRNA-Leu (UUR) gene associated with the Melas subgroup of mitochondrial encephalomyopathies. Nature 348: 651-653, 1990
-
(1990)
Nature
, vol.348
, pp. 651-653
-
-
Goto, Y.1
Nonaka, I.2
Horai, S.3
-
10
-
-
0027996170
-
Prevalence of maternally inherited diabetes and deafness in diabetic populations in the Netherlands
-
Hart L'T, Lemkes HHPJ, Heine RJ, Stolk RP, Feskens EJM, Jansen JJ, van der Does FEE, Grobbee DE, Kromhout D, van den Ouweland JMW, Maassen JA: Prevalence of maternally inherited diabetes and deafness in diabetic populations in the Netherlands. Diabetologia 37: 1169-1170, 1994
-
(1994)
Diabetologia
, vol.37
, pp. 1169-1170
-
-
Hart, L.T.1
Lemkes, H.H.P.J.2
Heine, R.J.3
Stolk, R.P.4
Feskens, E.J.M.5
Jansen, J.J.6
Van der Does, F.E.E.7
Grobbee, D.E.8
Kromhout, D.9
Van den Ouweland, J.M.W.10
Maassen, J.A.11
-
11
-
-
0029960177
-
Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging
-
Hart L'T, Jansen JJ, Lemkes HHPJ, de Knijff P, Maassen JA: Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging. Human Mutation, 7: 193-197, 1996
-
(1996)
Human Mutation
, vol.7
, pp. 193-197
-
-
Hart, L.T.1
Jansen, J.J.2
Lemkes, H.H.P.J.3
De Knijff, P.4
Maassen, J.A.5
-
12
-
-
0023883150
-
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
-
Holt IJ, Harding AE, Morgan-Hughes JA: Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. Nature 331: 717-719, 1988
-
(1988)
Nature
, vol.331
, pp. 717-719
-
-
Holt, I.J.1
Harding, A.E.2
Morgan-Hughes, J.A.3
-
13
-
-
0023896248
-
Two mutant alleles of the insulin receptor gene in a patient with extreme insulin resistance
-
Kadowaki T, Bevins CL, Cama A, Ojaama K, Marcus-Samuels B, Kadowaki H, Beitz L, McKeon C, Taylor SI: Two mutant alleles of the insulin receptor gene in a patient with extreme insulin resistance. Science 240: 787-790, 1988
-
(1988)
Science
, vol.240
, pp. 787-790
-
-
Kadowaki, T.1
Bevins, C.L.2
Cama, A.3
Ojaama, K.4
Marcus-Samuels, B.5
Kadowaki, H.6
Beitz, L.7
McKeon, C.8
Taylor, S.I.9
-
14
-
-
0027474253
-
Mitochondrial gene mutation and insulin deficient type of diabetes mellitus
-
Kadowaki H, Tobe K, Mori Y, Sakura H, Sakuta R, Nonaka I, Hagura R, Yazaki Y, Akanuma Y, Kadowaki T: Mitochondrial gene mutation and insulin deficient type of diabetes mellitus. Lancet 341: 893-894, 1993
-
(1993)
Lancet
, vol.341
, pp. 893-894
-
-
Kadowaki, H.1
Tobe, K.2
Mori, Y.3
Sakura, H.4
Sakuta, R.5
Nonaka, I.6
Hagura, R.7
Yazaki, Y.8
Akanuma, Y.9
Kadowaki, T.10
-
15
-
-
0028328317
-
A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA
-
Kadowaki T, Kadowaki H, Mori Y, Tobe K, Sakuta R, Suzuki Y, Tanabe Y, Sakura H, Awata T, Goto Y, Hayakawa T, Matsuoka K, Kawamori R, Kamada T, Horai S, Nonaka I, Hagura R, Akanuma Y, Yazaki Y: A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA. New Eng J Med 330: 962-968, 1994
-
(1994)
New Eng J Med
, vol.330
, pp. 962-968
-
-
Kadowaki, T.1
Kadowaki, H.2
Mori, Y.3
Tobe, K.4
Sakuta, R.5
Suzuki, Y.6
Tanabe, Y.7
Sakura, H.8
Awata, T.9
Goto, Y.10
Hayakawa, T.11
Matsuoka, K.12
Kawamori, R.13
Kamada, T.14
Horai, S.15
Nonaka, I.16
Hagura, R.17
Akanuma, Y.18
Yazaki, Y.19
-
16
-
-
0028242793
-
Insulin resistance in mitochondrial gene mutation
-
Kanamori A, Tanaka, K, Umezawa S: Insulin resistance in mitochondrial gene mutation. Diabetes Care 17: 778-779, 1994
-
(1994)
Diabetes Care
, vol.17
, pp. 778-779
-
-
Kanamori, A.1
Tanaka, K.2
Umezawa, S.3
-
17
-
-
0028258021
-
Mitochondrial diabetes mellitus: Prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu, UUR) gene mutation in Japanese patients
-
Katagiri H, Asano T, Ishihara H, Inukai K, Anai M, Yamagouchi T, Tsukuda K, Kikuchi M, Kitaoka H, Ohsawa N, Yazaki Y, Oka Y: Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu, UUR) gene mutation in Japanese patients. Diabetologia 37: 504-510, 1994
-
(1994)
Diabetologia
, vol.37
, pp. 504-510
-
-
Katagiri, H.1
Asano, T.2
Ishihara, H.3
Inukai, K.4
Anai, M.5
Yamagouchi, T.6
Tsukuda, K.7
Kikuchi, M.8
Kitaoka, H.9
Ohsawa, N.10
Yazaki, Y.11
Oka, Y.12
-
18
-
-
0028891842
-
Diabetes mellitus carrying a mutation in mitochondrial tRNA (Leu, UUR) gene
-
Kishimoto M, Hashiramoto M, Araki S: Diabetes mellitus carrying a mutation in mitochondrial tRNA (Leu, UUR) gene. Diabetologia 38: 193-200, 1995
-
(1995)
Diabetologia
, vol.38
, pp. 193-200
-
-
Kishimoto, M.1
Hashiramoto, M.2
Araki, S.3
-
19
-
-
0024436947
-
A leucine to proline mutation in the insulin receptor in a family with insulin resistance
-
Klinkhamer MP, Groen NA, Van der Zon GCM, Lindhout D, Sandkuyl LA, Krans HMJ, Moller W, Maassen JA: A leucine to proline mutation in the insulin receptor in a family with insulin resistance. EMBO J 8: 2503-2507, 1989
-
(1989)
EMBO J
, vol.8
, pp. 2503-2507
-
-
Klinkhamer, M.P.1
Groen, N.A.2
Van der Zon, G.C.M.3
Lindhout, D.4
Sandkuyl, L.A.5
Krans, H.M.J.6
Moller, W.7
Maassen, J.A.8
-
20
-
-
0002872316
-
Empirical risk figures for first degree relatives of non-insulin dependent diabetics
-
Köbberling J, Tattersall R (eds)
-
Köbberling J, Tillil H: Empirical risk figures for first degree relatives of non-insulin dependent diabetics. In Köbberling J, Tattersall R (eds) The genetics of diabetes Academic Press London, pp 201-209., 1982
-
(1982)
The Genetics of Diabetes Academic Press London
, pp. 201-209
-
-
Köbberling, J.1
Tillil, H.2
-
21
-
-
0003182407
-
Maternal inherited diabetes-deafness of the young (MIDDY), a new mitochondrial syndrome
-
Lemkes HHPJ, de Vijlder M, Struyvenberg P, Van der Kamp JJP, Fröhlich M: Maternal inherited diabetes-deafness of the young (MIDDY), a new mitochondrial syndrome. Diabetologia 32: 509A, 1989
-
(1989)
Diabetologia
, vol.32
-
-
Lemkes, H.H.P.J.1
De Vijlder, M.2
Struyvenberg, P.3
Van der Kamp, J.J.P.4
Fröhlich, M.5
-
22
-
-
0002806616
-
Genetics of diabetes mellitus
-
Alberti KGMM, DeFronzo RA, Keen H, Zimmet P (eds) Wiley, Chichester
-
LaVadheim CM Rotter JI: Genetics of diabetes mellitus. In: Alberti KGMM, DeFronzo RA, Keen H, Zimmet P (eds) International textbook of diabetes mellitus. Wiley, Chichester, pp 31-98, 1992
-
(1992)
International Textbook of Diabetes Mellitus
, pp. 31-98
-
-
Lavadheim, C.M.1
Rotter, J.I.2
-
23
-
-
0027268052
-
Mitochondrial gene mutation in islet cell antibody positive patients who were initially non-insulin-dependent diabetes
-
Oka Y, Katagiri H, Yazaki Y, Murase T, Kabayashi T: Mitochondrial gene mutation in islet cell antibody positive patients who were initially non-insulin-dependent diabetes. Lancet 342: 527-528, 1993
-
(1993)
Lancet
, vol.342
, pp. 527-528
-
-
Oka, Y.1
Katagiri, H.2
Yazaki, Y.3
Murase, T.4
Kabayashi, T.5
-
24
-
-
0027968580
-
The high prevalence of the diabetic patients with a mutation in the mitochondrial gene in Japan
-
Otabe S, Sakura H, Shimokawa K, et al.: The high prevalence of the diabetic patients with a mutation in the mitochondrial gene in Japan. J Clin Endocrinol Metab 79: 768-771, 1994
-
(1994)
J Clin Endocrinol Metab
, vol.79
, pp. 768-771
-
-
Otabe, S.1
Sakura, H.2
Shimokawa, K.3
-
25
-
-
0026462744
-
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA
-
Reardon W, Ross RJM, Sweeney MG, Luxon LM, Pembrey ME, Harding AE, Trembath RC: Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA. Lancet 340: 1376-1379, 1992
-
(1992)
Lancet
, vol.340
, pp. 1376-1379
-
-
Reardon, W.1
Ross, R.J.M.2
Sweeney, M.G.3
Luxon, L.M.4
Pembrey, M.E.5
Harding, A.E.6
Trembath, R.C.7
-
26
-
-
0027477373
-
Mitochondrial gene mutations and diabetes mellitus
-
Sue CM, Holmeswaker DJ, Morris JGL, Boyages SC, Crimmins DS, Byrne E: Mitochondrial gene mutations and diabetes mellitus. Lancet 341, 437-438, 1993
-
(1993)
Lancet
, vol.341
, pp. 437-438
-
-
Sue, C.M.1
Holmeswaker, D.J.2
Morris, J.G.L.3
Boyages, S.C.4
Crimmins, D.S.5
Byrne, E.6
-
27
-
-
0027939581
-
Pancreatic beta cell secretory defect associated with mitochondrial point mutation of the tRNA(Leu, UUR) gene: A study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke like episodes (MELAS)
-
Suzuki S, Hinokio Y, Onoda M. Matsumoto M, Ohtomo M, Kawasaki H, Satoh Y, Akai H, Abe K, Miyabayashi S, Kawasaki E, Nagataki S, Toyota T: Pancreatic beta cell secretory defect associated with mitochondrial point mutation of the tRNA(Leu, UUR) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke like episodes (MELAS). Diabetologia 37: 818-825, 1994
-
(1994)
Diabetologia
, vol.37
, pp. 818-825
-
-
Suzuki, S.1
Hinokio, Y.2
Matsumoto M, O.M.3
Ohtomo, M.4
Kawasaki, H.5
Satoh, Y.6
Akai, H.7
Abe, K.8
Miyabayashi, S.9
Kawasaki, E.10
Nagataki, S.11
Toyota, T.12
-
28
-
-
0016244025
-
Mild familial diabetes with dominant inheritance
-
Tattersal RB: Mild familial diabetes with dominant inheritance Q J Med 43: 339-357, 1974
-
(1974)
Q J Med
, vol.43
, pp. 339-357
-
-
Tattersal, R.B.1
-
29
-
-
0026761432
-
Mutations in the insulin receptor gene
-
Taylor SI, Cama A, Accili D, Barbetti F, Quon MJ, de la Luz Sierra M, Suzuki Y, Koller E, Levi-Toledano R, Wertheimer E, Moncada VY, Kadowaki H, Kadowaki T: Mutations in the insulin receptor gene. Endocrine Rev 13: 566-595, 1992
-
(1992)
Endocrine Rev
, vol.13
, pp. 566-595
-
-
Taylor, S.I.1
Cama, A.2
Accili, D.3
Barbetti, F.4
Quon, M.J.5
De la Luz Sierra, M.6
Suzuki, Y.7
Koller, E.8
Levi-Toledano, R.9
Wertheimer, E.10
Moncada, V.Y.11
Kadowaki, H.12
Kadowaki, T.13
-
30
-
-
0026906885
-
Mutation in mitochondrial tRNA (Leu, UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
-
Van den Ouweland JMW, Lemkes HHPJ, Ruitenbeek W, Sandkuyl LA, de Vijlder MF, Struyvenberg PAA, van de Kamp JJP, Maassen JA: Mutation in mitochondrial tRNA (Leu, UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nature Genet 1: 368-371, 1992
-
(1992)
Nature Genet
, vol.1
, pp. 368-371
-
-
Van den Ouweland, J.M.W.1
Lemkes, H.2
Ruitenbeek, W.3
Sandkuyl, L.A.4
De Vijlder, M.F.5
Paa, S.6
Van de Kamp, J.J.P.7
Maassen, J.A.8
-
31
-
-
0028365102
-
Maternally inherited diabetes and deafness (MIDD) is a distict subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu, UUR) gene
-
Van den Ouweland JMW, Lemkes HHPJ, Trembath RC, Ross R, Velho G, Cohen D, Froguel Ph, Maassen JA: Maternally inherited diabetes and deafness (MIDD) is a distict subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu, UUR) gene. Diabetes 43: 746-751, 1994
-
(1994)
Diabetes
, vol.43
, pp. 746-751
-
-
Van den Ouweland, J.M.W.1
Lemkes, H.H.P.J.2
Trembath, R.C.3
Ross, R.4
Velho, G.5
Cohen, D.6
Froguel, Ph.7
Maassen, J.A.8
-
33
-
-
0028907342
-
A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q
-
Vaxillaire M, Boccio V, Phillipi C, Vigoureux J, Terwilliger P, Passa JS, Beckmann G, Velho G, Lathrop GM, Froguel Ph: A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q. Nature Genet. 9: 418-423, 1995
-
(1995)
Nature Genet.
, vol.9
, pp. 418-423
-
-
Vaxillaire, M.1
Boccio, V.2
Phillipi, C.3
Vigoureux, J.4
Terwilliger, P.5
Passa, J.S.6
Beckmann, G.7
Velho, G.8
Lathrop, G.M.9
Froguel, Ph.10
-
34
-
-
0026562918
-
Nonsense mutations in the glucokinase gene causes early-onset non-insulin dependent diabetes mellitus
-
Vionet N, Stoffel M, Takeda J, Yasuda K, Bell GI, Zouali H, Lesage S, Velho G, Iris F, Passa P, Froguel Ph: Nonsense mutations in the glucokinase gene causes early-onset non-insulin dependent diabetes mellitus. Nature 356: 721-722, 1992
-
(1992)
Nature
, vol.356
, pp. 721-722
-
-
Vionet, N.1
Stoffel, M.2
Takeda, J.3
Yasuda, K.4
Bell, G.I.5
Zouali, H.6
Lesage, S.7
Velho, G.8
Iris, F.9
Passa, P.10
Froguel, Ph.11
-
35
-
-
0026639928
-
Human glucokinase gene: Isolation, characterization and identification of two missense mutations linked to early-onset non-insulin dependent (type 2) diabetes mellitus
-
Stoffel M, Froguel Ph, Takeda J, Zhouali H, Vionnet N, Nishi S, Weber IT, Harrison RW, Pilkis SJ, Lesage S, Vaxilliaire M, Velho G, Sun F, Iris F, Passa P, Cohen D, Bell GI: Human glucokinase gene: Isolation, characterization and identification of two missense mutations linked to early-onset non-insulin dependent (type 2) diabetes mellitus. Proc Natl Acad Sci USA 89: 7698-7702, 1992
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 7698-7702
-
-
Stoffel, M.1
Froguel, Ph.2
Takeda, J.3
Zhouali, H.4
Vionnet, N.5
Nishi, S.6
Weber, I.T.7
Harrison, R.W.8
Pilkis, S.J.9
Lesage, S.10
Vaxilliaire, M.11
Velho, G.12
Sun, F.13
Iris, F.14
Passa, P.15
Cohen, D.16
Bell, G.I.17
-
36
-
-
0024242545
-
Mitochondrial DNA mutations associated with Leber's hereditary optic neuropathy
-
Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, Elsas LJ, Nikoskelainen EK: Mitochondrial DNA mutations associated with Leber's hereditary optic neuropathy. Science 242: 1427-1430, 1988
-
(1988)
Science
, vol.242
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lott, M.T.3
Hodge, J.A.4
Schurr, T.G.5
Lezza, A.M.6
Elsas, L.J.7
Nikoskelainen, E.K.8
-
37
-
-
0026624980
-
Diseases of the mitochondrial DNA
-
Wallace DC: Diseases of the mitochondrial DNA. Annu Rev Biochem 61: 1175-1212, 1992
-
(1992)
Annu Rev Biochem
, vol.61
, pp. 1175-1212
-
-
Wallace, D.C.1
-
38
-
-
0028233947
-
Mitochondrial DNA mutations in diseases of energy metabolism
-
Wallace DC: Mitochondrial DNA mutations in diseases of energy metabolism, J. Bioenerg Biomembr 26: 241-250, 1994
-
(1994)
J. Bioenerg Biomembr
, vol.26
, pp. 241-250
-
-
Wallace, D.C.1
-
39
-
-
0029071513
-
Mitochondrial DNA mutations in human degenerative diseases and aging
-
Wallace DC, Shoffner JM, Trounce I, Brown MP, Ballinger SW, Corraldebrinski M, Horton T, Jun AS, Lott MT: Mitochondrial DNA mutations in human degenerative diseases and aging. Biochem Biophys Acta 1271: 141-151, 1995
-
(1995)
Biochem Biophys Acta
, vol.1271
, pp. 141-151
-
-
Wallace, D.C.1
Shoffner, J.M.2
Trounce, I.3
Brown, M.P.4
Ballinger, S.W.5
Corraldebrinski, M.6
Horton, T.7
Jun, A.S.8
Lott, M.T.9
-
40
-
-
0028978105
-
Mutation in the mitochondrial tRNA(Leu) at position 3243 and spontaneous abortions in Japanese women attending a clinic for diabetic pregancy
-
Yanagisawa K, Uchigata Y, Sanaka M, et al: Mutation in the mitochondrial tRNA(Leu) at position 3243 and spontaneous abortions in Japanese women attending a clinic for diabetic pregancy. Diabetologia 38: 809-815, 1994
-
(1994)
Diabetologia
, vol.38
, pp. 809-815
-
-
Yanagisawa, K.1
Uchigata, Y.2
Sanaka, M.3
-
41
-
-
0028104288
-
Congestive hart failure in mitochondrial diabetes mellitus
-
Yoshida R, Ishida Y, Hozumi T, Ueno H, Kishimoto M, Kasuga M, Kazumi T: Congestive hart failure in mitochondrial diabetes mellitus. Lancet 344: 1375, 1994
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(1994)
Lancet
, vol.344
, pp. 1375
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Yoshida, R.1
Ishida, Y.2
Hozumi, T.3
Ueno, H.4
Kishimoto, M.5
Kasuga, M.6
Kazumi, T.7
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