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Article

Novel mutation of the myelin P0 gene in a CMT1B family.

Human mutation - 1 Jan 1997

Sorour E, MacMillan J, Upadhyaya M

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Identifiers

PMID: 8990016
DOI: 10.1002/(SICI)1098-1004(1997)9:1<74::AID-HUMU16>3.0.CO;2-M

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Novel mutation of the myelin P0 gene in a CMT1B family.PMID 8990016Read ↗

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