2 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 28356563 | Homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome. | 2017 Jul | 1 |
2 | 25609768 | Fe/S protein assembly gene IBA57 mutation causes hereditary spastic paraplegia. | 2015 Feb 17 | 1 |