MeSH Browser

MeSH Supplementary: Xeroderma Pigmentosum, Complementation Group B
Unique ID: C562590
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562590
Entry Term(s): Xeroderma Pigmentosum, Group B
Registry Numbers: 0
Heading Mapped to: *Xeroderma Pigmentosum
Frequency: 2
Note: mutation in ERCC3 excision repair gene, which is also found in Cockayne syndrome
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Xeroderma Pigmentosum, Complementation Group B MeSH Supplementary Concept Data 2025