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Q24313568-156B6A75-8B2F-401C-8E2F-DD2A5A83C6CA
Q24313568-156B6A75-8B2F-401C-8E2F-DD2A5A83C6CA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24313568-156B6A75-8B2F-401C-8E2F-DD2A5A83C6CA
Dominant GDAP1 mutations cause predominantly mild CMT phenotypes
P2860
Q24313568-156B6A75-8B2F-401C-8E2F-DD2A5A83C6CA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24313568-156B6A75-8B2F-401C-8E2F-DD2A5A83C6CA
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wasDerivedFrom
f23d56ac6a5cdf7f646f3496e8062008cc022b4d
P2860
Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies