A novel XK gene mutation in a Taiwanese family with McLeod syndrome-Reference-Cited by-同舟云学术

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A novel XK gene mutation in a Taiwanese family with McLeod syndrome

Published:2014-05 Issue:1-2 Volume:340 Page:221-224
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Chen Pei-Yun,Lai Szu-Chia,Yang Chih-Chao,Lee Ming-Jen,Chiu Yen-Hui,Yan Sui-Hing,Lu Chin-Song,Yeh Tu-Hsueh

Funder

Chang Gung Medical Foundation, Taiwan

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference20 articles.

1. Neuroacanthocytosis syndromes;Jung;Orphanet J Rare Dis,2011

2. McLeod neuroacanthocytosis: genotype and phenotype;Danek;Ann Neurol,2001

3. Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein;Ho;Cell,1994

4. Point mutations causing the McLeod phenotype;Russo;Transfusion,2002

5. The chorea of McLeod syndrome;Danek;Mov Disord,2001

Cited by 7 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. Xp21 DNA microdeletion syndrome in a Chinese family: clinical features show retinitis pigmentosa and chronic granuloma;Frontiers in Genetics;2024-01-26

2. McLeod Syndrome in a Commercial Airline Pilot;Aerospace Medicine and Human Performance;2021-09-01

3. Novel c.435delC mutation in XK gene found in a Taiwanese patient with McLeod syndrome;Transfusion;2021-02-10

4. Nosology and Phenomenology of Psychosis in Movement Disorders;Movement Disorders Clinical Practice;2020-01-07

5. McLeod syndrome: Five new pedigrees with novel mutations;Parkinsonism & Related Disorders;2019-07

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