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Q35234076-C8DE79CB-76D1-45F1-9205-D7F125DE3BE6
Q35234076-C8DE79CB-76D1-45F1-9205-D7F125DE3BE6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35234076-C8DE79CB-76D1-45F1-9205-D7F125DE3BE6
Neurofilament light polypeptide gene N98S mutation in mice leads to neurofilament network abnormalities and a Charcot-Marie-Tooth Type 2E phenotype.
P2860
Q35234076-C8DE79CB-76D1-45F1-9205-D7F125DE3BE6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35234076-C8DE79CB-76D1-45F1-9205-D7F125DE3BE6
rank
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type
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Statement
wasDerivedFrom
d21e953af452cbfed4cac49189318d0b564edd79
P2860
A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy.