المؤلفون: Dilek Colak, Mazhor Al-Dosary, Hesham Aldhalaan, Namik Kaya, Maha Al-Rasheed, Maysoon Alsagob, Hadeel Jaber, Musaad Abukhalid, Hadeel Alkofide, Mohammed A. AlMuhaizea, Rawan Almass, Laila AlQuait, Albandary Al-Bakheet, Felwa Binhumaid, Hanouf Aldeeb

المصدر: Annals of Human Genetics. 86:34-44

مصطلحات موضوعية: Genetics, education.field_of_study, Movement disorders, business.industry, Genetic counseling, Population, Saudi Arabia, Ataxia Telangiectasia Mutated Proteins, Disease, medicine.disease, Compound heterozygosity, Ataxia Telangiectasia, Consanguinity, Phenotype, Mutation, Ataxia-telangiectasia, medicine, Humans, Oculomotor apraxia, medicine.symptom, Allele, education, business, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24bd77b7f7aeaca1e3711976331bf0c5
https://doi.org/10.1111/ahg.12445