X‑linked adrenoleukodystrophy caused by maternal ABCD1 mutation and paternal X chromosome inactivation-Reference-Cited by-同舟云学术

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X‑linked adrenoleukodystrophy caused by maternal ABCD1 mutation and paternal X chromosome inactivation

Published:2022-07-12 Issue:3 Volume:24 Page:
ISSN:1792-0981
Container-title:Experimental and Therapeutic Medicine
language:
Short-container-title:Exp Ther Med

Author:

Li Zhen¹,Lai Guangrui²

Affiliation:

1. Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, Liaoning 110004, P.R. China

2. Department of Clinical Genetics, Shengjing Hospital of China Medical University, Shenyang, Liaoning 110004, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Immunology and Microbiology (miscellaneous),General Medicine

Reference26 articles.

1. The changing face of adrenoleukodystrophy;Zhu;Endocr Rev,2020

2. Deciphering the modifiers for phenotypic variability of X-linked adrenoleukodystrophy;Palakuzhiyil;World J Biol Chem,2020

3. Phenotype assignment in symptomatic female carriers of X-linked adrenoleukodystrophy;Schmidt;J Neurol,2001

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

5. Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms;Salsano;Orphanet J Rare Dis,2012

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. Sex‐specific newborn screening for X‐linked adrenoleukodystrophy;Journal of Inherited Metabolic Disease;2022-10-26

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