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

por Al-Temaimi, Rabeah Abbas, Al-Enezi, Anwar, Al-Serri, Ahmad, Al-Roughani, Raed, Al-Mulla, Fahd
Publicado 2015

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

por Acar, Sezer, BinEssa, Huda A., Demir, Korcan, Al-Rijjal, Roua A., Zou, Minjing, Çatli, Gönül, Anık, Ahmet, Al-Enezi, Anwar F., Özışık, Seçil, Al-Faham, Manar S. A., Abacı, Ayhan, Dündar, Bumin, Kattan, Walaa E., Alsagob, Maysoon, Kavukçu, Salih, Tamimi, Hamdi E., Meyer, Brian F., Böber, Ece, Shi, Yufei
Publicado 2018