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Q41381963-C29AA0B2-FCE8-4F95-BFD7-F0498C59945E
Q41381963-C29AA0B2-FCE8-4F95-BFD7-F0498C59945E
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http://www.wikidata.org/entity/statement/Q41381963-C29AA0B2-FCE8-4F95-BFD7-F0498C59945E
Screening for SH3TC2 gene mutations in a series of demyelinating recessive Charcot-Marie-Tooth disease (CMT4).
P2860
Q41381963-C29AA0B2-FCE8-4F95-BFD7-F0498C59945E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41381963-C29AA0B2-FCE8-4F95-BFD7-F0498C59945E
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16d7704d34477830b2cd8f86198e8e2cda59f764
P2860
The allelic spectrum of Charcot-Marie-Tooth disease in over 17,000 individuals with neuropathy.