Identification and functional study of novel PLP1 mutations in Chinese patients with Pelizaeus–Merzbacher disease-Reference-Cited by-同舟云学术

Identification and functional study of novel PLP1 mutations in Chinese patients with Pelizaeus–Merzbacher disease

Published:2015-09 Issue:8 Volume:37 Page:797-802
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Xie Han,Feng Hongchun,Ji Jinhua,Wu Ye,Kou Liping,Li Dongxiao,Ji Haoran,Wu Xiru,Niu Zhengping,Wang Jingmin,Jiang Yuwu

Funder

Project of the Science and Technology Ministry of China

National Natural Science Foundation of China

National Key Research Project

Beijing Natural Science Foundation

Publisher

Elsevier BV

Subject

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

Reference30 articles.

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4. X-linked spastic paraplegia and Pelizaeus–Merzbacher disease are allelic disorders at the proteolipid protein locus;Saugier-Veber;Nat Genet,1994

5. Magnetic resonance imaging and computed tomography in Pelizaeus–Merzbacher disease;Caro;Magn Reson Imaging,1990

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3. Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report;BMC Pediatrics;2018-02-27

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