MERRF-Like Phenotype Associated with a Rare Mitochondrial tRNAIle Mutation (m.4284 G>A)-Reference-Cited by-同舟云学术

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MERRF-Like Phenotype Associated with a Rare Mitochondrial tRNAIle Mutation (m.4284 G>A)

Published:2011-07-15 Issue:04 Volume:42 Page:148-151
ISSN:0174-304X
Container-title:Neuropediatrics
language:en
Short-container-title:Neuropediatrics

Author:

Hahn A.¹,Schänzer A.¹,Neubauer B.A.¹,Gizewski E.¹,Ahting U.²,Rolinski B.³

Affiliation:

1. University of Giessen

2. Institute of Clinical Chemistry

3. Elblab Zentrum für LaborMedizin

Publisher

Georg Thieme Verlag KG

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0031-1283167.pdf

Cited by 11 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. Myoclonic epilepsy with ragged red fibers syndrome associated with mitochondrial 3302A>G mutation in the MT‑TL1 gene: A case report;Experimental and Therapeutic Medicine;2023-01-04

2. Maneuvering Mitochondria for Better Understanding of Therapeutic Potential of mtDNA Mutation;Mutagenesis [Working Title];2021-03-23

3. Deregulated Mitochondrial DNA in Diseases;DNA and Cell Biology;2020-08-01

4. Pathogenic Mitochondria DNA Mutations: Current Detection Tools and Interventions;Genes;2020-02-12

5. Myoclonus Epilepsy with Ragged-Red Fibers (MERRF);Diagnosis and Management of Mitochondrial Disorders;2019

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