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Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families.
Khalaf-Nazzal, Reham; Dweikat, Imad; Maree, Mosab; Alawneh, Maysa; Barahmeh, Myassar; Doulani, Rasha T; Qrareya, Mohammad; Qadi, Mohammad; Dudin, Anwar.
Affiliation
  • Khalaf-Nazzal R; Faculty of Medicine, Arab American University of Palestine, Jenin, Palestine. Electronic address: reham.nazzal@aaup.edu.
  • Dweikat I; Faculty of Medicine, Arab American University of Palestine, Jenin, Palestine.
  • Maree M; Medicine Department, Faculty of Medicine and Health Sciences, An-Najah National University, and An-Najah National University Hospital, Nablus, Palestine.
  • Alawneh M; Medicine Department, Faculty of Medicine and Health Sciences, An-Najah National University, and An-Najah National University Hospital, Nablus, Palestine.
  • Barahmeh M; Biomedical Sciences Department, Faculty of Medicine and Health Sciences, An-Najah National University, Nablus, Palestine.
  • Doulani RT; Clinical Sciences Department, Faculty of Medicine and Health Sciences, An-Najah National University, Nablus, Palestine.
  • Qrareya M; Clinical Sciences Department, Faculty of Medicine and Health Sciences, An-Najah National University, Nablus, Palestine.
  • Qadi M; Biomedical Sciences Department, Faculty of Medicine and Health Sciences, An-Najah National University, Nablus, Palestine.
  • Dudin A; Pediatric Neurology Outpatient Clinic, Ramallah, Palestine.
Brain Dev ; 44(7): 454-461, 2022 Aug.
Article in En | MEDLINE | ID: mdl-35440380
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hereditary Central Nervous System Demyelinating Diseases / Cysts / Membrane Proteins Type of study: Prognostic_studies Limits: Humans Language: En Journal: Brain Dev Year: 2022 Document type: Article
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hereditary Central Nervous System Demyelinating Diseases / Cysts / Membrane Proteins Type of study: Prognostic_studies Limits: Humans Language: En Journal: Brain Dev Year: 2022 Document type: Article