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Q24313568-DE6A0759-39BD-46E5-83E4-12140DFD9E10
Q24313568-DE6A0759-39BD-46E5-83E4-12140DFD9E10
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24313568-DE6A0759-39BD-46E5-83E4-12140DFD9E10
Dominant GDAP1 mutations cause predominantly mild CMT phenotypes
P921
Q24313568-DE6A0759-39BD-46E5-83E4-12140DFD9E10
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24313568-DE6A0759-39BD-46E5-83E4-12140DFD9E10
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
17da9be1f8890cd10616e848aec6b571eb80d078
P921
mitochondrial fusion