An unusually mild case of biotin-thiamine-responsive basal ganglia disease-Reference-Cited by-同舟云学术

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An unusually mild case of biotin-thiamine-responsive basal ganglia disease

Published:2023-12 Issue: Volume:37 Page:101004
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Lail Gurnoor,Blaser Susan,Inbar-Feigenberg Michal

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference8 articles.

1. Treatable Leigh-like encephalopathy presenting in adolescence;Fassone;BMJ Case Rep.,2013

2. Biotin-thiamine-responsive basal ganglia disease. 2013 Nov 21 [Updated 2020 Aug 20];Tabarki,1993

3. SLC19A3 gene defects sorting the phenotype and acronyms: review;Alfadhel;Neuropediatrics.,2018

4. Report of the largest Chinese cohort with SLC19A3 gene defect and literature review;Wang;Front. Genet.,2021

5. A wide spectrum of clinical and brain MRI findings in patients with SLC19A3 mutations;Yamada;BMC Med. Genet.,2010

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. Biotin Homeostasis and Human Disorders: Recent Findings and Perspectives;International Journal of Molecular Sciences;2024-06-14

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