Association of CTG repeats and the 1-kbAlu insertion/deletion polymorphism at the myotonin protein kinase gene in the Japanese population suggests a common Eurasian origin of the myotonic dystrophy mutation
Keyword(s):
1995 ◽
Vol 97
(4)
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pp. S131
Keyword(s):
Keyword(s):
1999 ◽
Vol 27
(17)
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pp. 3534-3542
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1999 ◽
Vol 22
(9)
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pp. 1271-1274
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Keyword(s):
1998 ◽
Vol 273
(15)
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pp. 9139-9147
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1995 ◽
Vol 6
(1)
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pp. 13-19
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