المؤلفون: Laetitia, Mavinga Mpola, Veronique, Kakiese, Mamy, Ngole Zita, Cathy, Songo Mbodo, Lumaka Zola, Aimé, Race, Valerie, Prosper, Lukusa Tshilobo, Devriendt, Koenraad

المصدر: European Journal of Medical Genetics, 65 (11), 104611 (2022-11)

مصطلحات موضوعية: DRCongo, Melanin, OCA, OCA2 gene, Membrane Transport Proteins, Cross-Sectional Studies, Democratic Republic of the Congo/epidemiology, Humans, Molecular Biology, Mutation, Albinism, Oculocutaneous/genetics, Membrane Transport Proteins/genetics, Albinism, Oculocutaneous, Democratic Republic of the Congo, Genetics, Genetics (clinical), General Medicine, Life sciences, Genetics & genetic processes, Human health sciences, Dermatology, Pediatrics, Sciences du vivant, Génétique & processus génétiques, Sciences de la santé humaine, Dermatologie, Pédiatrie

Relation: https://api.elsevier.com/content/article/PII:S1769721222001926?httpAccept=text/xml; 10.1016/j.ejmg.2022.104611; urn:issn:1769-7212; urn:issn:1878-0849

URL الوصول: https://orbi.uliege.be/handle/2268/299600

المؤلفون: Laetitia Mavinga Mpola

نوع المادة: eBook.

تصنيفات: MEDICAL / General

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