Improving post-natal detection of mitochondrial DNA mutations-Reference-Cited by-同舟云学术

Improving post-natal detection of mitochondrial DNA mutations

Published:2020-09-20 Issue:10 Volume:20 Page:1003-1008
ISSN:1473-7159
Container-title:Expert Review of Molecular Diagnostics
language:en
Short-container-title:Expert Review of Molecular Diagnostics

Author:

Barcia Giulia¹,Assouline Zahra¹,Magen Maryse¹,Pennisi Alessandra¹²,Rötig Agnès²,Munnich Arnold¹²,Bonnefont Jean-Paul¹²,Steffann Julie¹²

Affiliation:

1. Université de Paris et Service de Génétique Moléculaire, Reference Center for Mitochondrial Diseases (CARAMMEL), Groupe Hospitalier Necker Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France

2. Laboratory for Genetics of Mitochondrial Disorders, INSERM U1163, Université Paris Descartes-Sorbonne Paris Cité, Institut Imagine, Paris, France

Publisher

Informa UK Limited

Subject

Genetics,Molecular Biology,Molecular Medicine,Pathology and Forensic Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/14737159.2020.1820326

Reference44 articles.

1. Minimum birth prevalence of mitochondrial respiratory chain disorders in children

2. A neurological perspective on mitochondrial disease

3. Mitochondrial genetics

4. Mitochondrial Genetics

5. Sequence and organization of the human mitochondrial genome

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