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Q28118945-AC17E592-4F67-46DF-83CA-2BDA20C540E0
Q28118945-AC17E592-4F67-46DF-83CA-2BDA20C540E0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28118945-AC17E592-4F67-46DF-83CA-2BDA20C540E0
De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)
P2860
Q28118945-AC17E592-4F67-46DF-83CA-2BDA20C540E0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28118945-AC17E592-4F67-46DF-83CA-2BDA20C540E0
rank
NormalRank
type
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Statement
wasDerivedFrom
e62153f1438589dadd7778f15c6e358d4b1dba14
P2860
Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.