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Q34999364-660085DD-21A4-4D67-9B1F-BADC0248607E
Q34999364-660085DD-21A4-4D67-9B1F-BADC0248607E
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Statement
http://www.wikidata.org/entity/statement/Q34999364-660085DD-21A4-4D67-9B1F-BADC0248607E
MFN2 mutations cause severe phenotypes in most patients with CMT2A.
P2860
Q34999364-660085DD-21A4-4D67-9B1F-BADC0248607E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34999364-660085DD-21A4-4D67-9B1F-BADC0248607E
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wasDerivedFrom
d8b6ef436eb94b752db96020f849d4dec44b9650
P2860
Complementation between mouse Mfn1 and Mfn2 protects mitochondrial fusion defects caused by CMT2A disease mutations.