-
1
-
-
17344363640
-
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
-
Bashir, R., Britton, S., Strachan, T., Keers, S., Vafiadaki, E., Lako, M., Richard, I., Marchand, S., Bourg, N., Argov, Z. et al. (1998) A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B. Nature Genet., 20, 37-42.
-
(1998)
Nature Genet.
, vol.20
, pp. 37-42
-
-
Bashir, R.1
Britton, S.2
Strachan, T.3
Keers, S.4
Vafiadaki, E.5
Lako, M.6
Richard, I.7
Marchand, S.8
Bourg, N.9
Argov, Z.10
-
2
-
-
17344365600
-
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
-
Liu, J., Aoki, M., Illa, I., Wu, C., Fardeau, M., Angelini, C., Serrano, C., Urtizberea, J.A., Hentati, F., Hamida, M.B. et al. (1998) Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Nature Genet., 20, 31-36.
-
(1998)
Nature Genet.
, vol.20
, pp. 31-36
-
-
Liu, J.1
Aoki, M.2
Illa, I.3
Wu, C.4
Fardeau, M.5
Angelini, C.6
Serrano, C.7
Urtizberea, J.A.8
Hentati, F.9
Hamida, M.B.10
-
3
-
-
0030477874
-
The phenotype of chromosome 2p-linked limb-girdle muscular dystrophy
-
Mahjneh, I., Passos-Bueno, M.R., Zatz, M., Vainzof, M., Marconi, G., Nashef, L., Bashir, R. and Bushby, K. (1996) The phenotype of chromosome 2p-linked limb-girdle muscular dystrophy. Neuromusc. Disord., 6, 483-490.
-
(1996)
Neuromusc. Disord.
, vol.6
, pp. 483-490
-
-
Mahjneh, I.1
Passos-Bueno, M.R.2
Zatz, M.3
Vainzof, M.4
Marconi, G.5
Nashef, L.6
Bashir, R.7
Bushby, K.8
-
4
-
-
0022634885
-
Autosomal recessive distal muscular dystrophy as a new type of progressive muscular dystrophy. Seventeen cases in eight families including an autopsied case
-
Miyoshi, K., Kawai, H., Iwasa, M., Kusaka, K. and Nishino, H. (1986) Autosomal recessive distal muscular dystrophy as a new type of progressive muscular dystrophy. Seventeen cases in eight families including an autopsied case. Brain, 109, 31-54.
-
(1986)
Brain
, vol.109
, pp. 31-54
-
-
Miyoshi, K.1
Kawai, H.2
Iwasa, M.3
Kusaka, K.4
Nishino, H.5
-
5
-
-
0031878338
-
Miyoshi myopathy in Saudi Arabia: Clinical, electrophysiological, histopathological and radiological features
-
Cupler, E.J., Bohlega, S., Hessler, R., McLean, D., Stigsby, B. and Ahmad, J. (1998) Miyoshi myopathy in Saudi Arabia: clinical, electrophysiological, histopathological and radiological features. Neuromusc. Disord., 8, 321-326.
-
(1998)
Neuromusc. Disord.
, vol.8
, pp. 321-326
-
-
Cupler, E.J.1
Bohlega, S.2
Hessler, R.3
McLean, D.4
Stigsby, B.5
Ahmad, J.6
-
6
-
-
0023132925
-
High serum levels of creatine kinase: Asymptomatic prelude to distal myopathy
-
Galassi, G., Rowland, L.P., Hays, A.P., Hopkins, L.C. and DiMauro, S. (1987) High serum levels of creatine kinase: asymptomatic prelude to distal myopathy. Musc. Nerve. 10, 346-350.
-
(1987)
Musc. Nerve.
, vol.10
, pp. 346-350
-
-
Galassi, G.1
Rowland, L.P.2
Hays, A.P.3
Hopkins, L.C.4
DiMauro, S.5
-
7
-
-
0028951204
-
Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14
-
Bejaoui, K., Hirabayashi, K., Hentati, F., Haines, J.L., Ben Hamida, C., Belal, S., Miller, R.G., McKenna-Yasek, D., Weissenbach, J., Rowland, L.P. et al. (1995) Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14. Neurology, 45, 768-772.
-
(1995)
Neurology
, vol.45
, pp. 768-772
-
-
Bejaoui, K.1
Hirabayashi, K.2
Hentati, F.3
Haines, J.L.4
Ben Hamida, C.5
Belal, S.6
Miller, R.G.7
McKenna-Yasek, D.8
Weissenbach, J.9
Rowland, L.P.10
-
8
-
-
0029057637
-
Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate region
-
Passos-Bueno, M.R., Bashir, R., Moreira, E.S., Vainzof, M., Marie, S.K., Vasquez, L., Iughetti, P., Bakker, E., Keers, S., Stephenson, A. et al. (1995) Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate region. Genomics, 27, 192-195.
-
(1995)
Genomics
, vol.27
, pp. 192-195
-
-
Passos-Bueno, M.R.1
Bashir, R.2
Moreira, E.S.3
Vainzof, M.4
Marie, S.K.5
Vasquez, L.6
Iughetti, P.7
Bakker, E.8
Keers, S.9
Stephenson, A.10
-
9
-
-
0032897762
-
Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)
-
Weiler, T., Bashir, R., Anderson, L.V., Davison, K., Moss, J.A., Britton, S., Nylen, E., Keers, S., Vafiadaki, E., Greenberg, C.R. et al. (1999) Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s). Hum. Mol. Genet., 8, 871-877.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 871-877
-
-
Weiler, T.1
Bashir, R.2
Anderson, L.V.3
Davison, K.4
Moss, J.A.5
Britton, S.6
Nylen, E.7
Keers, S.8
Vafiadaki, E.9
Greenberg, C.R.10
-
10
-
-
0019067646
-
Caenorhabditis elegans fertilization-defective mutants with abnormal sperm
-
Argon, Y. and Ward, S. (1980) Caenorhabditis elegans fertilization-defective mutants with abnormal sperm. Genetics, 96, 413-433.
-
(1980)
Genetics
, vol.96
, pp. 413-433
-
-
Argon, Y.1
Ward, S.2
-
11
-
-
0019848568
-
Sperm morphogenesis in wild-type and fertilization-defective mutants of Caenorhabditis elegans
-
Ward, S., Argon, Y. and Nelson, G.A. (1981) Sperm morphogenesis in wild-type and fertilization-defective mutants of Caenorhabditis elegans. J. Cell Biol., 91, 26-44.
-
(1981)
J. Cell Biol.
, vol.91
, pp. 26-44
-
-
Ward, S.1
Argon, Y.2
Nelson, G.A.3
-
12
-
-
0030972880
-
A nematode gene required for sperm vesicle fusion
-
Achanzar, W.E. and Ward, S. (1997) A nematode gene required for sperm vesicle fusion. J. Cell Sci., 110, 1073-1081.
-
(1997)
J. Cell Sci.
, vol.110
, pp. 1073-1081
-
-
Achanzar, W.E.1
Ward, S.2
-
14
-
-
0022458044
-
Cloning and expression of multiple protein kinase C cDNAs
-
Knopf, J.L., Lee, M.H., Sultzman, L.A., Kriz, R.W., Loomis, C.R., Hewick, R.M. and Bell, R.M. (1986) Cloning and expression of multiple protein kinase C cDNAs. Cell, 46, 491-502.
-
(1986)
Cell
, vol.46
, pp. 491-502
-
-
Knopf, J.L.1
Lee, M.H.2
Sultzman, L.A.3
Kriz, R.W.4
Loomis, C.R.5
Hewick, R.M.6
Bell, R.M.7
-
15
-
-
0022504365
-
Multiple, distinct forms of bovine and human protein kinase C suggest diversity in cellular signaling pathways
-
Coussens, L., Parker, P.J., Rhee, L., Yang-Feng, T.L., Chen, E., Waterfield, M.D., Francke, U. and Ullrich, A. (1986) Multiple, distinct forms of bovine and human protein kinase C suggest diversity in cellular signaling pathways. Science, 233, 859-866.
-
(1986)
Science
, vol.233
, pp. 859-866
-
-
Coussens, L.1
Parker, P.J.2
Rhee, L.3
Yang-Feng, T.L.4
Chen, E.5
Waterfield, M.D.6
Francke, U.7
Ullrich, A.8
-
16
-
-
0025270739
-
Phospholipid binding by a synaptic vesicle protein homologous to the regulatory region of protein kinase C
-
Perin, M.S., Fried, V.A., Mignery, G.A., Jahn, R. and Sudhof, T.C. (1990) Phospholipid binding by a synaptic vesicle protein homologous to the regulatory region of protein kinase C. Nature, 345, 260-263.
-
(1990)
Nature
, vol.345
, pp. 260-263
-
-
Perin, M.S.1
Fried, V.A.2
Mignery, G.A.3
Jahn, R.4
Sudhof, T.C.5
-
18
-
-
0028989281
-
Ca(2+)-dependent and -independent activities of neural and non-neural synaptotagmins
-
Li, C., Ullrich, B., Zhang, J.Z., Anderson, R.G., Brose, N. and Sudhof, T.C. (1995) Ca(2+)-dependent and -independent activities of neural and non-neural synaptotagmins. Nature, 375, 594-599.
-
(1995)
Nature
, vol.375
, pp. 594-599
-
-
Li, C.1
Ullrich, B.2
Zhang, J.Z.3
Anderson, R.G.4
Brose, N.5
Sudhof, T.C.6
-
19
-
-
0032955751
-
Dysferlin is a plasma membrane protein and is expressed early in human development
-
Anderson, L.V., Davison, K., Moss, J.A., Young, C., Cullen, M.J., Walsh, J., Johnson, M.A., Bashir, R., Britton, S., Keers, S. et al. (1999) Dysferlin is a plasma membrane protein and is expressed early in human development. Hum. Mol. Genet., 8, 855-861.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 855-861
-
-
Anderson, L.V.1
Davison, K.2
Moss, J.A.3
Young, C.4
Cullen, M.J.5
Walsh, J.6
Johnson, M.A.7
Bashir, R.8
Britton, S.9
Keers, S.10
-
20
-
-
0032947634
-
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a non-syndromic form of deafness
-
Yasunaga, S., Grati, M., Cohen-Salmon, M., El-Amraoui, A., Mustapha, M., Salem, N., El-Zir, E., Loiselet, J. and Petit, C. (1999) A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a non-syndromic form of deafness. Nature Genet., 21, 363-369.
-
(1999)
Nature Genet.
, vol.21
, pp. 363-369
-
-
Yasunaga, S.1
Grati, M.2
Cohen-Salmon, M.3
El-Amraoui, A.4
Mustapha, M.5
Salem, N.6
El-Zir, E.7
Loiselet, J.8
Petit, C.9
-
21
-
-
0028353499
-
Acid sphingomyelinase possesses a domain homologous to its activator proteins: Saposins B and D
-
Ponting, C.P. (1994) Acid sphingomyelinase possesses a domain homologous to its activator proteins: saposins B and D. Protein Sci., 3, 359-361.
-
(1994)
Protein Sci.
, vol.3
, pp. 359-361
-
-
Ponting, C.P.1
-
22
-
-
0029865117
-
Cytotoxic T cells: More weapons for new targets?
-
Tschopp, J. and Hofmann, K. (1996) Cytotoxic T cells: more weapons for new targets? Trends Microbiol., 4, 91-94,
-
(1996)
Trends Microbiol.
, vol.4
, pp. 91-94
-
-
Tschopp, J.1
Hofmann, K.2
-
23
-
-
0342789258
-
-
Duesterhoeft, A., Lauber, J., Mewes, H.W., Gassenhuber, J. and Wiemann, S. (1999) GenBank accession no. AL096713.1.
-
(1999)
GenBank Accession No. AL096713.1
-
-
Duesterhoeft, A.1
Lauber, J.2
Mewes, H.W.3
Gassenhuber, J.4
Wiemann, S.5
-
24
-
-
10544234620
-
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies
-
Vainzof, M., Passos-Bueno, M.R., Canovas, M., Moreira, E.S., Pavanello, R.C., Marie, S.K., Anderson, L.V., Bonnemann, C.G., McNally, E.M., Nigro, V. et al. (1996) The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies. Hum. Mol. Genet., 5, 1963-1969.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1963-1969
-
-
Vainzof, M.1
Passos-Bueno, M.R.2
Canovas, M.3
Moreira, E.S.4
Pavanello, R.C.5
Marie, S.K.6
Anderson, L.V.7
Bonnemann, C.G.8
McNally, E.M.9
Nigro, V.10
-
25
-
-
0024353559
-
The molecular basis of muscular dystrophy in the mdx mouse: A point mutation
-
Sicinski, P., Geng, Y., Ryder-Cook, A.S., Barnard, E.A., Darlison, M.G. and Barnard, P.J. (1989) The molecular basis of muscular dystrophy in the mdx mouse: a point mutation. Science, 244, 1578-1580.
-
(1989)
Science
, vol.244
, pp. 1578-1580
-
-
Sicinski, P.1
Geng, Y.2
Ryder-Cook, A.S.3
Barnard, E.A.4
Darlison, M.G.5
Barnard, P.J.6
-
26
-
-
0032494165
-
Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin
-
Hack, A.A., Ly, C.T., Jiang, F., Clendenin, C.J., Sigrist, K.S., Wollmann, R.L. and McNally, E.M. (1998) Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin. J. Cell Biol., 142, 1279-1287.
-
(1998)
J. Cell Biol.
, vol.142
, pp. 1279-1287
-
-
Hack, A.A.1
Ly, C.T.2
Jiang, F.3
Clendenin, C.J.4
Sigrist, K.S.5
Wollmann, R.L.6
McNally, E.M.7
-
27
-
-
0029964897
-
A critical evaluation of resting intracellular free calcium regulation in dystrophic mdx muscle
-
Hopf, F.W., Turner, P.R., Denetclaw, W.F.Jr, Reddy, P. and Steinhardt, R.A. (1996) A critical evaluation of resting intracellular free calcium regulation in dystrophic mdx muscle. Am. J. Physiol., 271, 1325-1339.
-
(1996)
Am. J. Physiol.
, vol.271
, pp. 1325-1339
-
-
Hopf, F.W.1
Turner, P.R.2
Denetclaw W.F., Jr.3
Reddy, P.4
Steinhardt, R.A.5
-
28
-
-
0025222219
-
Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin
-
Fong, P.Y., Turner, P.R., Denetclaw, W.F. and Steinhardt, R.A. (1990) Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin. Science, 250, 673-676.
-
(1990)
Science
, vol.250
, pp. 673-676
-
-
Fong, P.Y.1
Turner, P.R.2
Denetclaw, W.F.3
Steinhardt, R.A.4
-
29
-
-
84965289894
-
Intracellular calcium and pathogenesis and antenatal diagnosis of Duchenne muscular dystrophy
-
Emery, A.E. and Burt, D. (1980) Intracellular calcium and pathogenesis and antenatal diagnosis of Duchenne muscular dystrophy. Br. Med. J., 280, 355-357.
-
(1980)
Br. Med. J.
, vol.280
, pp. 355-357
-
-
Emery, A.E.1
Burt, D.2
-
30
-
-
0028168590
-
Synaptotagmin I is a high affinity receptor for clathrin AP-2: Implications for membrane recycling
-
Zhang, J.Z., Davletov, B.A., Sudhof, T.C. and Anderson, R.G. (1994) Synaptotagmin I is a high affinity receptor for clathrin AP-2: implications for membrane recycling. Cell, 78, 751-760.
-
(1994)
Cell
, vol.78
, pp. 751-760
-
-
Zhang, J.Z.1
Davletov, B.A.2
Sudhof, T.C.3
Anderson, R.G.4
-
31
-
-
0029589647
-
A possible docking and fusion particle for synaptic transmission
-
Schiavo, G., Gmachl, M.J., Stenbeck, G., Sollner, T.H. and Rothman, J.E. (1995) A possible docking and fusion particle for synaptic transmission. Nature, 378, 733-736.
-
(1995)
Nature
, vol.378
, pp. 733-736
-
-
Schiavo, G.1
Gmachl, M.J.2
Stenbeck, G.3
Sollner, T.H.4
Rothman, J.E.5
-
33
-
-
0029670820
-
Distinct Ca(2+)-dependent properties of the first and second C2-domains of synaptotagmin I. J
-
Sugita, S., Hata, Y. and Sudhof, T.C. (1996) Distinct Ca(2+)-dependent properties of the first and second C2-domains of synaptotagmin I. J. Biol. Chem., 271, 1262-1265.
-
(1996)
Biol. Chem.
, vol.271
, pp. 1262-1265
-
-
Sugita, S.1
Hata, Y.2
Sudhof, T.C.3
-
34
-
-
0032849111
-
Muscle degeneration without mechanical injury in sarcoglycan deficiency
-
Hack, A.A., Cordier, L., Shoturma, D.I., Lam, M.Y., Sweeney, H.L. and McNally, E.M. (1999) Muscle degeneration without mechanical injury in sarcoglycan deficiency. Proc. Natl Acad. Sci. USA. 96, 10723-10728.
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 10723-10728
-
-
Hack, A.A.1
Cordier, L.2
Shoturma, D.I.3
Lam, M.Y.4
Sweeney, H.L.5
McNally, E.M.6
-
35
-
-
0029874852
-
Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy
-
Nagano, A., Koga, R., Ogawa, M., Kurano, Y., Kawada, J., Okada, R., Hayashi, Y.K., Tsukahara, T. and Arahata, K. (1996) Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy. Nature Genet., 12, 254-259.
-
(1996)
Nature Genet.
, vol.12
, pp. 254-259
-
-
Nagano, A.1
Koga, R.2
Ogawa, M.3
Kurano, Y.4
Kawada, J.5
Okada, R.6
Hayashi, Y.K.7
Tsukahara, T.8
Arahata, K.9
-
36
-
-
0010397284
-
The Emery-Dreifuss muscular dystrophy protein, emerin, is a nuclear membrane protein
-
Manilal, S., Nguyen, T.M., Sewry, C.A. and Morris, G.E. (1996) The Emery-Dreifuss muscular dystrophy protein, emerin, is a nuclear membrane protein. Hum. Mol. Genet., 5, 801-808.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 801-808
-
-
Manilal, S.1
Nguyen, T.M.2
Sewry, C.A.3
Morris, G.E.4
-
37
-
-
0343640698
-
Heart-specific localization of emerin: New insights into Emery-Dreifuss muscular dystrophy
-
Cartegni, L., di Barletta, M.R., Barresi, R., Squarzoni, S., Sabatelli, P., Maraldi, N., Mora, M., Di Blasi, C., Cornelio, F., Merlini, L. et al. (1997) Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy. Hum. Mol. Genet., 6, 2257-2264.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2257-2264
-
-
Cartegni, L.1
Di Barletta, M.R.2
Barresi, R.3
Squarzoni, S.4
Sabatelli, P.5
Maraldi, N.6
Mora, M.7
Di Blasi, C.8
Cornelio, F.9
Merlini, L.10
-
38
-
-
0032977685
-
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
-
Bonne, G., Di Barletta, M.R., Varnous, S., Becane, H.M., Hammouda, E.H., Merlini, L., Muntoni, F., Greenberg, C.R., Gary, F., Urtizberea, J.A. et al. (1999) Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nature Genet., 21, 285-288.
-
(1999)
Nature Genet.
, vol.21
, pp. 285-288
-
-
Bonne, G.1
Di Barletta, M.R.2
Varnous, S.3
Becane, H.M.4
Hammouda, E.H.5
Merlini, L.6
Muntoni, F.7
Greenberg, C.R.8
Gary, F.9
Urtizberea, J.A.10
-
39
-
-
0031105607
-
GATA-5: A transcriptional activator expressed in a novel temporally and spatially-restricted pattern during embryonic development
-
Morrisey, E.E., Ip, H.S., Tang, Z., Lu, M.M. and Parmacek, M.S. (1997) GATA-5: a transcriptional activator expressed in a novel temporally and spatially-restricted pattern during embryonic development. Dev. Biol., 183, 21-36.
-
(1997)
Dev. Biol.
, vol.183
, pp. 21-36
-
-
Morrisey, E.E.1
Ip, H.S.2
Tang, Z.3
Lu, M.M.4
Parmacek, M.S.5
-
40
-
-
0027959491
-
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
-
McNally, E.M., Yoshida, M., Mizuno, Y., Ozawa, E. and Kunkel, L.M. (1994) Human adhalin is alternatively spliced and the gene is located on chromosome 17q21. Proc. Natl Acad. Sci. USA, 91, 9690-9694.
-
(1994)
Proc. Natl Acad. Sci. USA
, vol.91
, pp. 9690-9694
-
-
McNally, E.M.1
Yoshida, M.2
Mizuno, Y.3
Ozawa, E.4
Kunkel, L.M.5
-
41
-
-
10344249872
-
Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy
-
McNally, E.M., Duggan, D., Gorospe, J.R., Bonnemann, C.G., Fanin, M., Pegoraro, E., Lidov, H.G., Noguchi, S., Ozawa, E., Finkel, R.S. et al. (1996) Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy. Hum. Mol. Genet., 5, 1841-1847.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1841-1847
-
-
McNally, E.M.1
Duggan, D.2
Gorospe, J.R.3
Bonnemann, C.G.4
Fanin, M.5
Pegoraro, E.6
Lidov, H.G.7
Noguchi, S.8
Ozawa, E.9
Finkel, R.S.10
-
42
-
-
0026067790
-
Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma
-
Ohlendieck, K., Ervasti, J.M., Snook, J.B. and Campbell, K.P. (1991) Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma. J. Cell Biol., 112, 135-148.
-
(1991)
J. Cell Biol.
, vol.112
, pp. 135-148
-
-
Ohlendieck, K.1
Ervasti, J.M.2
Snook, J.B.3
Campbell, K.P.4
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