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Q24311502-F51B848B-B4F7-4120-8F58-AA0ADF4ACC98
Q24311502-F51B848B-B4F7-4120-8F58-AA0ADF4ACC98
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Statement
http://www.wikidata.org/entity/statement/Q24311502-F51B848B-B4F7-4120-8F58-AA0ADF4ACC98
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene
P2860
Q24311502-F51B848B-B4F7-4120-8F58-AA0ADF4ACC98
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24311502-F51B848B-B4F7-4120-8F58-AA0ADF4ACC98
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wasDerivedFrom
04bccb2ce5abdb35c621368cb4c3ed6b069a74b0
P2860
The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication