KBTBD13 protein, human MeSH Supplementary Concept Data 2025

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MeSH Supplementary: KBTBD13 protein, human
Unique ID: C555066
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C555066
Registry Numbers: 0
Heading Mapped to: *Muscle Proteins
Frequency: 13
Note: mutation leads to nemaline myopathy with cores; RefSeq NM_001101362
Source: Am J Hum Genet 2010 Dec 10;87(6):842-7
Date of Entry: 2011/01/16
Revision Date: 2011/01/16

KBTBD13 protein, human Preferred

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