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Q47190201-C65AF95B-B44C-4956-B5A8-7DE3C2E0E4EE
Q47190201-C65AF95B-B44C-4956-B5A8-7DE3C2E0E4EE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47190201-C65AF95B-B44C-4956-B5A8-7DE3C2E0E4EE
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency.
P2860
Q47190201-C65AF95B-B44C-4956-B5A8-7DE3C2E0E4EE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47190201-C65AF95B-B44C-4956-B5A8-7DE3C2E0E4EE
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wasDerivedFrom
33bb1aeac69c4ba6272ee9b1749ca2e523d6727a
P2860
In vivo characterization of human myofibrillar myopathy genes in zebrafish.