Screening for SH3TC2
gene mutations in a series of demyelinating recessive Charcot-Marie-Tooth disease (CMT4)
2016 ◽
Vol 21
(3)
◽
pp. 142-149
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2010 ◽
Vol 52
(2)
◽
pp. 177-183
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Keyword(s):
2008 ◽
Vol 53
(6)
◽
pp. 529-533
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Keyword(s):
2001 ◽
Vol 49
(2)
◽
pp. 245-249
◽
2004 ◽
Vol 219
(1-2)
◽
pp. 95-100
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Keyword(s):
1996 ◽
Vol 7
(1)
◽
pp. 36-45
◽
Keyword(s):
2010 ◽
Vol 14
(1)
◽
pp. 3-7
◽
Keyword(s):