CYP2U1: An emerging treatable neurometabolic disease with cerebral folate deficiency in 2 Chinese brothers-Reference-Cited by-同舟云学术

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CYP2U1: An emerging treatable neurometabolic disease with cerebral folate deficiency in 2 Chinese brothers

Published:2024-03 Issue: Volume:38 Page:101023
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Wong Sheila Suet-Na,Yuen Liz Yuet-Ping,Kan Elaine,Blau Nenad,Rodenburg Richard,Lam Ching-wan,Wong Virginia Chun-Nei,Mochel Fanny,Wevers Ron A.,Fung Cheuk-Wing

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference12 articles.

1. Classification of the hereditary ataxias and paraplegias;Harding;Lancet.,1983

2. Recent advances in hereditary spastic paraplegia;Tallaksen;Curr. Opin. Neurol.,2001

3. Advances in the hereditary spastic paraplegias;Fink;Exp. Neurol.,2003

4. Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia;Tesson;Am. J. Hum. Genet.,2012

5. Hereditary spastic paraplegia;Murala;Neurol. Sci.,2021

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. A Homozygous Variant in NAA60 Is Associated with Primary Familial Brain Calcification;Movement Disorders;2024-09-04

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