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Q52146944-DB25AAE8-23A0-4320-A4C5-BB5613E875BA
Q52146944-DB25AAE8-23A0-4320-A4C5-BB5613E875BA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52146944-DB25AAE8-23A0-4320-A4C5-BB5613E875BA
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.
P2860
Q52146944-DB25AAE8-23A0-4320-A4C5-BB5613E875BA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52146944-DB25AAE8-23A0-4320-A4C5-BB5613E875BA
rank
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type
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wasDerivedFrom
10ed9cc3e368c00ba5e6efc3be755604591e75b5
P2860
MFN2 mutations cause severe phenotypes in most patients with CMT2A.