MeSH Browser

MeSH Supplementary: FKBP14 protein, human
Unique ID: C572897
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C572897
Registry Numbers: EC 5.2.1.8
Heading Mapped to: *Peptidylprolyl Isomerase
Frequency: 22
Note: mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss
Source: Am J Hum Genet. 2012 Feb 10;90(2):201-16
Indexing Information: Ehlers-Danlos Syndrome
Date of Entry: 2012/06/21
Revision Date: 1955/01/01

FKBP14 protein, human MeSH Supplementary Concept Data 2025