المؤلفون: Kefah Al-Qa'qa', Ali Al-Hawamdeh, Wajdi Amayreh, Buthaina Al Rababah, Hebah Deebajah, Saied A. Jaradat, Maha Karam, Paul Hoff Backe, Batool Al-Zoubi

المصدر: Meta Gene. 10:81-85

مصطلحات موضوعية: 0301 basic medicine, Proband, Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Mutation, Maple syrup urine disease, nutritional and metabolic diseases, BCKDHB, BCKDHA, Biology, medicine.disease, medicine.disease_cause, 03 medical and health sciences, Exon, 030104 developmental biology, medicine, Missense mutation, Gene, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e67c2856e6c57aeecae2429df43c6d4
https://doi.org/10.1016/j.mgene.2015.10.002