Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiency

European Journal of Human Genetics, Published online: 20 May 2021; doi:10.1038/s41431-021-00887-wConsolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiency

Source: European Journal of Human Genetics - May 20, 2021 Category: Genetics & Stem Cells Authors: Siying Lin James Fasham Fida ’ Al-Hijawi Nouar Qutob Adam Gunning Joseph S. Leslie Lucy McGavin Nishanka Ubeyratna Wisam Baker Ramez Zeid Peter D. Turnpenny Andrew H. Crosby Emma L. Baple Reham Khalaf-Nazzal Source Type: research