المؤلفون: Tammy Gillis, James S. Acierno, Marcy E. MacDonald, Eiman Al-Yamani, Wenqi Zeng, Pinar T. Ozand, Susan A. Slaugenhaupt, James F. Gusella

المصدر: American journal of human genetics. 77(1)

مصطلحات موضوعية: Male, medicine.medical_specialty, Encephalopathy, Biotin, Genes, Recessive, Biology, Basal Ganglia Diseases, Internal medicine, Basal ganglia, Genetics, medicine, Missense mutation, Humans, Genetics(clinical), Basal ganglia disease, Genetics (clinical), Dystonia, Base Sequence, Putamen, Membrane Transport Proteins, Articles, medicine.disease, Pedigree, Endocrinology, Chromosomes, Human, Pair 2, SLC19A3, Mutation, SLC19A2, biology.protein, Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::041aa1c3aa040c3d002429305549a8e0
https://pubmed.ncbi.nlm.nih.gov/15871139