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Q24633906-1034EE66-76C9-4C19-9A18-E1C8F6648B3D
Q24633906-1034EE66-76C9-4C19-9A18-E1C8F6648B3D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24633906-1034EE66-76C9-4C19-9A18-E1C8F6648B3D
A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy
P2860
Q24633906-1034EE66-76C9-4C19-9A18-E1C8F6648B3D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24633906-1034EE66-76C9-4C19-9A18-E1C8F6648B3D
rank
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type
BestRank
Statement
wasDerivedFrom
626b014fb55ffa12ace041d2ff07e358afa6a42c
P2860
Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.