MeSH Browser

MeSH Supplementary: PHF6 protein, human
Unique ID: C502542
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C502542
Entry Term(s): PDH finger protein 6, human
Previous Indexing: *Carrier Proteins (2005-2020)
Heading Mapped to: *Repressor Proteins
Frequency: 70
Note: mutations in PHF6 lead to mild Borjeson-Forssman-Lehmann syndrome, RefSeq NM_032458
Source: J Med Genet 2004 Oct;41(10):778-83
Indexing Information: Zinc Fingers
Date of Entry: 2005/08/03
Revision Date: 2019/12/20

PHF6 protein, human MeSH Supplementary Concept Data 2024