MeSH Browser

MeSH Supplementary: MEOX1 protein, human
Unique ID: C525671
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C525671
Registry Numbers: 0
Heading Mapped to: *Transcription Factors; *Homeodomain Proteins
Frequency: 20
Note: No mutations were identified in the PAX1 and MEOX1 exons or flanking intronic sequences, excluding them as likely causative genes for diaphanospondylodysostosis
Source: Am J Med Genet A. 2007 Oct 1;143(19):2292-302
Date of Entry: 2008/01/11
Revision Date: 2019/12/18

MEOX1 protein, human MeSH Supplementary Concept Data 2025