Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotype-Reference-Cited by-同舟云学术

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Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotype

Published:2021-11 Issue: Volume:92 Page:7-12
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Hsu Shao-Lun,Chen Ying-Hao,Chou Cheng-Ta,Chou Ying-Tsen,Tsai Yu-Shuen,Hsiao Cheng-Tsung,Liao Yi-Chu,Lee Yi-Chung

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference29 articles.

1. Adrenoleukodystrophy - neuroendocrine pathogenesis and redefinition of natural history;Kemp;Nat. Rev. Endocrinol.,2016

2. The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane protein;Mosser;Hum. Mol. Genet.,1994

3. Evolution of phenotypes in adult male patients with X-linked adrenoleukodystrophy;van Geel;Ann. Neurol.,2001

4. X-linked adrenoleukodystrophy in women: a cross-sectional cohort study;Engelen;Brain,2014

5. Natural history of X-linked adrenoleukodystrophy in Japan;Suzuki;Brain Dev.,2005

Cited by 1 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. Investigating KIF1A mutations in a Taiwanese cohort with hereditary spastic paraplegia;Parkinsonism & Related Disorders;2022-10

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