Haya Aldossari

Haya Aldossari

Alfaisal University - Riyadh / Saudi Arabia
Natural Sciences / Molecular Biology & Genetics
AD Scientific Index ID: 5478384
جامعة الفيصل
person_outline Haya Aldossari's MOST POPULAR ARTICLES
1-) Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c. 2761C> T Gene 536 (1), 217-220, 2014
2-) A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family European Journal of Medical Genetics 56 (1), 43-45, 2013
3-) The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population Genetics in Medicine 17 (9), 719-725, 2015
4-) Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia BMC Medical Genetics 20, 1-6, 2019
5-) Novel mutations in TGM1 and ABCA12 cause autosomal recessive congenital ichthyosis in five Saudi families International Journal of Dermatology 55 (6), 673-679, 2016