Missense mutations are frequent in the gene for X-chromosomal adrenoleukodystrophy (ALD)-Reference-Cited by-同舟云学术

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Missense mutations are frequent in the gene for X-chromosomal adrenoleukodystrophy (ALD)

Published:1994 Issue:10 Volume:3 Page:1903-1905
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Fuchs Sigrid,Sarde Claude Olivier,Wedemann Heike,Schwinger Eberhard,Mandel Jean Louis,Gal Andreas

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/3/10/1903/1880104/3-10-1903.pdf

Cited by 59 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. A female adult-onset X-ALD patient with pure cerebellar symptoms:a case report;Heliyon;2024-08

2. Genotypic and phenotypic heterogeneity among Chinese pediatric genetic white matter disorders;Italian Journal of Pediatrics;2023-11-19

3. X-linked cerebral adrenoleukodystrophy;BMJ Case Reports;2023-10

4. Identification of Two Novel Mutations of ABCD1 Gene in Pedigrees with X-Linked Adrenoleukodystrophy and Review of the Literature;International Journal of Endocrinology;2022-02-07

5. Structure insights of the human peroxisomal ABC transporter ALDP;2021-09-25

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