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Q55316890-0E10C6A3-CEA7-475C-8938-97C24426D4A9
Q55316890-0E10C6A3-CEA7-475C-8938-97C24426D4A9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55316890-0E10C6A3-CEA7-475C-8938-97C24426D4A9
Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies.
P2860
Q55316890-0E10C6A3-CEA7-475C-8938-97C24426D4A9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55316890-0E10C6A3-CEA7-475C-8938-97C24426D4A9
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wasDerivedFrom
0f7b41bef835ec511c44ac065dc7454afcac6a2e
P2860
Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization.