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Q33681015-5EBC769C-768B-4A29-90F2-DE1DE95C1B43
Q33681015-5EBC769C-768B-4A29-90F2-DE1DE95C1B43
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Statement
http://www.wikidata.org/entity/statement/Q33681015-5EBC769C-768B-4A29-90F2-DE1DE95C1B43
Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1 disease and HNPP.
P2860
Q33681015-5EBC769C-768B-4A29-90F2-DE1DE95C1B43
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33681015-5EBC769C-768B-4A29-90F2-DE1DE95C1B43
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wasDerivedFrom
2513f0bb7616734cd4245cda02b4cc1d47563fce
P2860
The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication