A Caucasian Family with the 3271 Mutation in Mitochondrial DNA-Reference-Cited by-同舟云学术

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A Caucasian Family with the 3271 Mutation in Mitochondrial DNA

Published:1994-08 Issue:2 Volume:52 Page:136-139
ISSN:0885-4505
Container-title:Biochemical Medicine and Metabolic Biology
language:en
Short-container-title:Biochemical Medicine and Metabolic Biology

Author:

Marie S.K.N.,Goto Y.,Passosbueno M.R.,Zatz M.,Carvalho A.A.S.,Carvalho M.,Levy J.A.,Palou V.B.,Campiotto S.,Horai S.,Nonaka I.

Publisher

Elsevier BV

Subject

Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 24 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. Epilepsy in mitochondrial diseases. Clinical lecture;Russian Journal of Child Neurology;2023-05-18

2. Genetic causes of stroke in young patients;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2019

3. Early onset cardiomyopathy associated with the mitochondrial tRNALeu(UUR) 3271T>C MELAS mutation;Biochemical and Biophysical Research Communications;2015-03

4. Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes in a Japanese child: Clinical, radiological and molecular genetic analysis;Egyptian Journal of Medical Human Genetics;2013-07

5. Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders: An overview study;Mitochondrial DNA;2013-01-09

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