Truncating mutation in intracellular phospholipase A1 gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54)
2015 · BMC Research Notes · 23 citations
https://doi.org/10.1186/s13104-015-1227-4
Claim or correct this author profile
Claim this profile or suggest corrections to the name, affiliation, bio, photo, or paper titles. Approved changes appear as verified CitedEvidence overlays.
20
Papers
392
Citations
11
h-index
11
i10-index
Hussein Sheikh Ali Mohamoud is an academic researcher from St Thomas' Hospital. The author has contributed to research in topics: Genomics and Rare Diseases & Genetics and Neurodevelopmental Disorders & Hereditary Neurological Disorders. The author has an h-index of 11, co-authored 17 publications.
Click to start Chat