NDUFAF5 variants manifest phenotypically heterogeneously-Reference-Cited by-同舟云学术

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NDUFAF5 variants manifest phenotypically heterogeneously

Published:2019-03 Issue: Volume:18 Page:8-9
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Finsterer Josef

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference4 articles.

1. Novel mutations in the mitochondrial complex I assembly gene NDUFAF5 reveal heterogeneous phenotypes;Simon;Mol Genet Metab.,2018

2. Stroke-like episodes in coenzyme-Q deficiency may respond to NO-precursors and non-mitochondrion-toxic antiepileptic drugs;Finsterer;Mol Genet Metab Rep,2018

3. The mitochondrial tRNA(Ala) T5655C mutation may modulate the phenotypic expression of tRNA(Met) and tRNA(Gln) A4401G mutation in a Han Chinese family with essential hypertension;Xu;Int. Heart J.,2017

4. Letter to the Editor: Endocrine compromise in mitochondrial disorders;Finsterer;J Endocr Soc,2018

Cited by 2 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. Reply;Ultrasound in Obstetrics & Gynecology;2024-03

2. Mitochondrial myopathy plus due to the variant m.586G > A in MT-TF;Molecular Genetics and Metabolism Reports;2019-12

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