Mutational Analyses of Taiwanese Kindred With X-linked Adrenoleukodystrophy-Reference-Cited by-同舟云学术

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Mutational Analyses of Taiwanese Kindred With X-linked Adrenoleukodystrophy

Published:2006-10 Issue:4 Volume:35 Page:250-256
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Chiu Hou-Chang,Liang Jao-Shwann,Wang Jinn-Shyan,Lu Jyh-Feng

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference35 articles.

1. A new human gene (DXS1357E) with ubiquitous expression, located in Xq28 adjacent to the adrenoleukodystrophy gene;Mosser;Genomics,1994

2. Adrenoleukodystrophy: New approaches to a neurodegenerative disease;Moser;JAMA,2005

3. Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls;Moser;Ann Neurol,1999

4. Peroxisomal lignoceroyl-CoA ligase deficiency in childhood adrenoleukodystrophy and adrenomyeloneuropathy;Lazo;Proc Natl Acad Sci USA,1988

5. Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters;Mosser;Nature,1993

Cited by 10 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. X-Linked Adrenoleukodystrophy;Emergency Neuro-ophthalmology;2018

2. Clinical, biochemical, neuroimaging and molecular findings of X-linked Adrenoleukodystrophy patients in South China;Metabolic Brain Disease;2015-08-12

3. Splicing defects in ABCD1 gene leading to both exon skipping and partial intron retention in X-linked adrenoleukodystrophy Tunisian patient;Neuroscience Research;2015-08

4. Molecular analysis in X-linked adrenoleukodystrophy patients: identification of a novel mutation;Metabolic Brain Disease;2014-05-01

5. Mutational Analyses on X-Linked Adrenoleukodystrophy Reveal a Novel Cryptic Splicing and Three Missense Mutations in the ABCD1 Gene;Pediatric Neurology;2013-09

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