Absence ofPMP22 coding region mutations in CMT1A duplication patients: Further evidence supporting gene dosage as a mechanism for charcot-marie-tooth disease type 1A
1996 ◽
Vol 8
(4)
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pp. 362-365
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Keyword(s):
2006 ◽
Vol 16
(3)
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pp. 183-187
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Keyword(s):
1993 ◽
Vol 306
(3)
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pp. 177-184
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Keyword(s):
2000 ◽
Vol 5
(4)
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pp. 240-240
Keyword(s):
1994 ◽
Vol 31
(10)
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pp. 811-815
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Keyword(s):