Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal development-Reference-Cited by-同舟云学术

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Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal development

Published:2006-03-29 Issue:10 Volume:43 Page:788-792
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Bouchet C,Steffann J,Corcos J,Monnot S,Paquis V,Rotig A,Lebon S,Levy P,Royer G,Giurgea I,Gigarel N,Benachi A,Dumez Y,Munnich A,Bonnefont J P

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Cited by 43 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

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2. Reproductive options in mitochondrial disease;Mitochondrial Diseases;2023

3. Enfermedades mitocondriales;EMC - Pediatría;2022-06

4. Molecular Genetics and Prenatal Diagnosis;Genetic Disorders and the Fetus;2021-04-20

5. A retrospective study on the efficacy of prenatal diagnosis for pregnancies at risk of mitochondrial DNA disorders;Genetics in Medicine;2021-04

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