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1دورية أكاديمية
المصدر: BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
مصطلحات موضوعية: X-ALD, X-linked Adrenoleukodystrophy, Neurodegenerative disorder, Rare disease, Mutation, ABCD1 gene, Medicine, Biology (General), QH301-705.5, Science (General), Q1-390
وصف الملف: electronic resource
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المؤلفون: D. Cheillan, H. Daoud-Tetouani, F. Z. Madani Benjelloun, Layachi Chabraoui, Yamna Kriouile
المصدر: BMC Research Notes
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)مصطلحات موضوعية: 0301 basic medicine, Adult, Male, X-ALD, Pediatrics, medicine.medical_specialty, ABCD1 gene, lcsh:Medicine, Metabolic disease, Disease, Asymptomatic, General Biochemistry, Genetics and Molecular Biology, Primary Adrenal Insufficiency, 03 medical and health sciences, 0302 clinical medicine, Rare Diseases, Clinical Protocols, X-linked adrenoleukodystrophy, medicine, Humans, Program Development, Psychiatry, lcsh:Science (General), Adrenoleukodystrophy, Child, lcsh:QH301-705.5, business.industry, lcsh:R, General Medicine, Neurodegenerative disorder, medicine.disease, Morocco, Research Note, 030104 developmental biology, lcsh:Biology (General), X-linked Adrenoleukodystrophy, Child, Preschool, Mutation, Program development, Female, medicine.symptom, business, Rare disease, 030217 neurology & neurosurgery, lcsh:Q1-390