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Q34999364-A2D74878-BB5C-4C41-9756-A70908CAF759
Q34999364-A2D74878-BB5C-4C41-9756-A70908CAF759
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Statement
http://www.wikidata.org/entity/statement/Q34999364-A2D74878-BB5C-4C41-9756-A70908CAF759
MFN2 mutations cause severe phenotypes in most patients with CMT2A.
P2860
Q34999364-A2D74878-BB5C-4C41-9756-A70908CAF759
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34999364-A2D74878-BB5C-4C41-9756-A70908CAF759
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wasDerivedFrom
2cb056f1db30fc92bbb4c02ec1e31954147398c9
P2860
Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations.