Anwar F Al-Enezi

Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis

Minjing Zou, Ali S. Alzahrani, Ali Al‐Odaib et al. · The Journal of Clinical Endocrinology & Metabolism · 2018 · 76 citations · Full text

The Association of Vitamin D Receptor Polymorphisms with Multiple Sclerosis in a Case-Control Study from Kuwait

Rabeah Al‐Temaimi, Anwar F Al-Enezi, Ahmad Al‐Serri et al. · PLoS ONE · 2015 · 50 citations · Full text

Nutrition, Autoimmune Disease, Disease Progression +15

Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3

Sezer Acar, Huda A. BinEssa, Korcan Demir et al. · PLoS ONE · 2018 · 33 citations · Full text

Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic rickets

Huda A. BinEssa, Minjing Zou, Anwar F Al-Enezi et al. · Bone · 2019 · 31 citations

Biology, Genetic Disorder, Splice-site Mutations +9

Mutational analysis of <i>PHEX</i>,<i> FGF23</i> and <i>CLCN5</i> in patients with hypophosphataemic rickets

Ayla Güven, Roua A. Al‐Rijjal, Huda A. BinEssa et al. · Clinical Endocrinology · 2017 · 29 citations