Mitochondrial DNA deletions detected by Multiplex Ligation-dependent Probe Amplification-Reference-Cited by-同舟云学术

Mitochondrial DNA deletions detected by Multiplex Ligation-dependent Probe Amplification

Published:2015-06-26 Issue:4 Volume:27 Page:2864-2867
ISSN:2470-1394
Container-title:Mitochondrial DNA Part A
language:en
Short-container-title:Mitochondrial DNA Part A

Author:

Mayorga Lía¹,Laurito Sergio R.¹,Loos Mariana A.²,Eiroa Hernán D.²,de Pinho Silvina²,Lubieniecki Fabiana²,Arroyo Hugo A.²,Pereyra Marcela F.³,Kauffman Marcelo A.⁴,Roqué María¹

Affiliation:

1. IHEM CCT-CONICET and National University of Cuyo, Mendoza, Argentina,

2. Garrahan Children’s Hospital, Buenos Aires, Argentina,

3. Notti Children’s Hospital, Mendoza, Argentina, and

4. J.M. Ramos Mejía General Hospital, Buenos Aires, Argentina

Publisher

Informa UK Limited

Subject

Genetics,Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.3109/19401736.2015.1053132

Reference9 articles.

1. Diagnostic Approach in Infants and Children with Mitochondrial Diseases

2. Comprehensive next-generation sequence analyses of the entire mitochondrial genome reveal new insights into the molecular diagnosis of mitochondrial DNA disorders

3. The in-depth evaluation of suspected mitochondrial disease

4. Mitochondrial DNA as a non-invasive biomarker: Accurate quantification using real time quantitative PCR without co-amplification of pseudogenes and dilution bias

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