Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene-Reference-Cited by-同舟云学术

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Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene

Published:1999-01 Issue:1 Volume:7 Page:45-51
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Verhoeven Kristien,Ensink Robbert JH,Tiranti Valeria,Huygen Patrick LM,Johnson David F,Schatteman Isabelle,Van Laer Lut,Verstreken Margriet,Van de Heyning Paul,Fischel-Ghodsian Nathan,Zeviani Massimo,Cremers Cor WRJ,Willems Patrick J,Van Camp Guy

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/5200247.pdf

Cited by 73 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. Usefulness of combined sequencing of the mitochondrial genome and a targeted panel of nuclear genes involved in mitochondrial diseases;Annales de Biologie Clinique;2021-02

2. Mitochondrial tRNASer(UCN) 7471delC may be a novel mutation associated with maternally transmitted hypertension;Irish Journal of Medical Science (1971 -);2019-11-27

3. Detection of mitochondrial transfer RNA (mt-tRNA) gene mutations in patients with idiopathic pulmonary fibrosis and sarcoidosis;Mitochondrion;2018-11

4. MERRF Classification: Implications for Diagnosis and Clinical Trials;Pediatric Neurology;2018-03

5. Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired Individuals;Annals of Human Genetics;2016-08-17

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