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Q34011184-6F7BBB38-4F6C-497B-ABF0-EF7A9F50DCDE
Q34011184-6F7BBB38-4F6C-497B-ABF0-EF7A9F50DCDE
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Statement
http://www.wikidata.org/entity/statement/Q34011184-6F7BBB38-4F6C-497B-ABF0-EF7A9F50DCDE
SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth disease
P2860
Q34011184-6F7BBB38-4F6C-497B-ABF0-EF7A9F50DCDE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34011184-6F7BBB38-4F6C-497B-ABF0-EF7A9F50DCDE
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wasDerivedFrom
a415356956a2ca5d7929de205b4207619d02e515
P2860
Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy.