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Q28118945-ABC44267-43F7-4248-876F-EA04A861C3CC
Q28118945-ABC44267-43F7-4248-876F-EA04A861C3CC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28118945-ABC44267-43F7-4248-876F-EA04A861C3CC
De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)
P2860
Q28118945-ABC44267-43F7-4248-876F-EA04A861C3CC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28118945-ABC44267-43F7-4248-876F-EA04A861C3CC
rank
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type
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Statement
wasDerivedFrom
e62153f1438589dadd7778f15c6e358d4b1dba14
P2860
The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication