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1دورية أكاديمية
المؤلفون: Paul Kabuyi Lumbala, Gloire Mbayabo, Mamy Nzita Ngole, Aimé Lumaka, Valerie Race, Gert Matthijs, Chris Van Geet, Prosper Tshilobo Lukusa, Koenraad Devriendt, Tite Minga Mikobi
المصدر: PLoS ONE, Vol 17, Iss 12, p e0278478 (2022)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1932-6203
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2دورية أكاديمية
المؤلفون: Laetitia MM; Department of Pediatrics, Faculty of Medicine, University of Kinshasa, Democratic Republic of the Congo, The; Centre for Human Genetics, Faculty of Medicine, University of Kinshasa, Democratic Republic of the Congo, The. Electronic address: mavingalaetitia@gmail.com., Veronique K; Department of Dermatology, Faculty of Medicine, University of Kinshasa, Democratic Republic of the Congo, The., Mamy NZ; Centre for Human Genetics, Faculty of Medicine, University of Kinshasa, Democratic Republic of the Congo, The., Cathy SM; Centre for Human Genetics, Faculty of Medicine, University of Kinshasa, Democratic Republic of the Congo, The., Aimé L; Department of Pediatrics, Faculty of Medicine, University of Kinshasa, Democratic Republic of the Congo, The; Centre for Human Genetics, Faculty of Medicine, University of Kinshasa, Democratic Republic of the Congo, The; Laboratory of Human Genetics, GIGA-R, University of Liège, Belgium., Race V; Center for Human Genetics, University Hospital, KU Leuven, Belgium., Prosper LT; Department of Pediatrics, Faculty of Medicine, University of Kinshasa, Democratic Republic of the Congo, The; Centre for Human Genetics, Faculty of Medicine, University of Kinshasa, Democratic Republic of the Congo, The; Center for Human Genetics, University Hospital, KU Leuven, Belgium., Devriendt K; Center for Human Genetics, University Hospital, KU Leuven, Belgium.
المصدر: European journal of medical genetics [Eur J Med Genet] 2022 Nov; Vol. 65 (11), pp. 104611. Date of Electronic Publication: 2022 Sep 16.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE
مواضيع طبية MeSH: Albinism, Oculocutaneous*/genetics , Membrane Transport Proteins*/genetics, Cross-Sectional Studies ; Democratic Republic of the Congo/epidemiology ; Humans ; Molecular Biology ; Mutation
SCR Disease Name: Oculocutaneous albinism type 2