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TMEM70 protein, human MeSH Supplementary Concept Data 2024


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 Preferred
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