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Q50194442-DA1B175E-58AB-46A1-8495-965894D9794E
Q50194442-DA1B175E-58AB-46A1-8495-965894D9794E
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Statement
http://www.wikidata.org/entity/statement/Q50194442-DA1B175E-58AB-46A1-8495-965894D9794E
Mitochondrial deficits and abnormal mitochondrial retrograde axonal transport play a role in the pathogenesis of mutant Hsp27-induced Charcot Marie Tooth Disease.
P2860
Q50194442-DA1B175E-58AB-46A1-8495-965894D9794E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50194442-DA1B175E-58AB-46A1-8495-965894D9794E
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wasDerivedFrom
26147e74081085e9614d4da5b22c18139cee7eb7
P2860
A mutation in the small heat-shock protein HSPB1 leading to distal hereditary motor neuronopathy disrupts neurofilament assembly and the axonal transport of specific cellular cargoes.