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Q24313568-D3FF4932-D753-417F-919A-E31658273934
Q24313568-D3FF4932-D753-417F-919A-E31658273934
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24313568-D3FF4932-D753-417F-919A-E31658273934
Dominant GDAP1 mutations cause predominantly mild CMT phenotypes
P2860
Q24313568-D3FF4932-D753-417F-919A-E31658273934
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24313568-D3FF4932-D753-417F-919A-E31658273934
rank
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wasDerivedFrom
f23d56ac6a5cdf7f646f3496e8062008cc022b4d
P2860
A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy.