Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans (Q36987175)
Jump to navigation
Jump to search
scientific article published on 5 November 2015
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans |
scientific article published on 5 November 2015 |
Statements
1 reference
Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans (English)
1 reference
Fowzan S Alkuraya
1 reference
Hanan E Shamseldin
1 reference
Laura L Smith
1 reference
Amal Kentab
1 reference
Hisham Alkhalidi
1 reference
Brady Summers
1 reference
Haifa Alsedairy
1 reference
Yong Xiong
1 reference
Vandana A Gupta
1 reference
5 November 2015
1 reference
1 reference
21-30
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference