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Mutation of the myelin P0 gene in Charcot-Marie-Tooth neuropathy type 1B.
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Publications
Mutation of the myelin P0 gene in Charcot-Marie-Tooth neuropathy type 1B.
Mutation of the myelin P0 gene in Charcot-Marie-Tooth neuropathy type 1B.
KH
K Hayasaka
K Hayasaka
GT
G Takada
G Takada
VI
V V Ionasescu
V V Ionasescu
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1 September 1993
Vol. 2
(9)
Abstract
No abstract available
Keywords
FUNCTION
NEUROPATHY
TOOTH
MYELIN
CHARCOT
MARIE
CONSTITUTES
P0 GENE
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