Back to Search
Start Over
Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial disease.
- Source :
- Human Molecular Genetics; Nov2022, Vol. 31 Issue 21, p3597-3612, 16p
- Publication Year :
- 2022
Details
- Language :
- English
- ISSN :
- 09646906
- Volume :
- 31
- Issue :
- 21
- Database :
- Complementary Index
- Journal :
- Human Molecular Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 159922586
- Full Text :
- https://doi.org/10.1093/hmg/ddac040