المؤلفون: Majid Alfadhel (5531333), Mohammed Almuqbil (10792740), Fuad Al Mutairi (9929217), Muhammad Umair (4062583), Mohammed Almannai (10792743), Malak Alghamdi (10657583), Hamad Althiyab (10792746), Rayyan Albarakati (10792749), Fahad A. Bashiri (6919919), Walaa Alshuaibi (10792752), Duaa Ba-Armah (10792755), Mohammed A. Saleh (10792758), Ali Al-Asmari (10792761), Eissa Faqeih (3416633), Waleed Altuwaijri (10792764), Ahmed Al-Rumayyan (10792767), Mohammed Ali Balwi (10792770), Faroug Ababneh (9138353), Abdulrahman Faiz Alswaid (10792773), Wafaa M. Eyaid (10792776), Naif A. M. Almontashiri (10304852), Amal Alhashem (3469799), Khalid Hundallah (10792779), Aida Bertoli-Avella (10792782), Peter Bauer (524851), Christian Beetz (499802), Muhammad Talal Alrifai (5531336), Ahmed Alfares (6800642), Brahim Tabarki (3469763)

مصطلحات موضوعية: Foetal Development and Medicine, Obstetrics and Gynaecology, Paediatrics, Paediatrics and Reproductive Medicine not elsewhere classified, leukodystrophy, Saudi Arabia, neurometabolic, metachromatic leukodystrophy, novel mutations

Relation: https://figshare.com/articles/figure/Image_1_The_Leukodystrophy_Spectrum_in_Saudi_Arabia_Epidemiological_Clinical_Radiological_and_Genetic_Data_jpg/14584947

الاتاحة: https://doi.org/10.3389/fped.2021.633385.s001