Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families-Reference-Cited by-同舟云学术

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Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families

Published:2022-08 Issue:7 Volume:44 Page:454-461
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Khalaf-Nazzal Reham,Dweikat Imad,Maree Mosab,Alawneh Maysa,Barahmeh Myassar,Doulani Rasha T.,Qrareya Mohammad,Qadi Mohammad,Dudin Anwar

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference22 articles.

1. Leukoencephalopathy with swelling and a discrepantly mild clinical course in eight children;van der Knaap;Ann Neurol,1995

2. Mutations of MLC1 (KIAA0027), encoding a putative membrane protein, cause megalencephalic leukoencephalopathy with subcortical cysts;Leegwater;Am J Hum Genet,2001

3. Ten novel mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cysts and a long-term follow-up research;Cao;PLoS ONE,2016

4. Megalencephalic leukoencephalopathy with subcortical cysts;Hamilton;Neurology,2018

5. Cystic leukoencephalopathy in a megalencephalic child: clinical and magnetic resonance imaging/magnetic resonance spectroscopy findings;Mejaski-Bosnjak;Pediatr Neurol,1997

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Megalencephalic leukoencephalopathy with subcortical cysts: a variant update and review of the literature;Frontiers in Genetics;2024-02-29

2. One person can make a difference: identification of people with a rare genetic lung disease;ERJ Open Research;2023-03

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