MeSH Browser

MeSH Supplementary: TMEM70 protein, human
Unique ID: C533106
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C533106
Heading Mapped to: *Membrane Proteins; *Mitochondrial Proteins
Frequency: 25
Note: mutations result in ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy; GenBank BC002748
Source: Nat Genet 2008 Nov;40(11):1288-90
Date of Entry: 2008/11/23
Revision Date: 2008/11/23

TMEM70 protein, human MeSH Supplementary Concept Data 2024