Hereditary motor and sensory neuropathy (HMSN) type X1 in an Argentinean family reveals independent GJB1/Cx32 mutations at the identical nucleotide position
1992 ◽
Vol 110
(1-2)
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pp. 121-130
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Keyword(s):
1980 ◽
Vol 43
(8)
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pp. 669-678
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Keyword(s):
2004 ◽
Vol 17
(2)
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pp. 290-299
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2004 ◽
Vol 115
(7)
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pp. 1689-1696
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