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Mitochondrial DNA Part A
DNA Mapping, Sequencing, and Analysis
Volume 27, 2016 - Issue 4
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Short Communication

Mitochondrial DNA deletions detected by Multiplex Ligation-dependent Probe Amplification

Lía MayorgaIHEM CCT-CONICET and National University of Cuyo, Mendoza, Argentina, Correspondence[email protected]
,
Sergio R. LauritoIHEM CCT-CONICET and National University of Cuyo, Mendoza, Argentina,
,
Mariana A. LoosGarrahan Children’s Hospital, Buenos Aires, Argentina,
,
Hernán D. EiroaGarrahan Children’s Hospital, Buenos Aires, Argentina,
,
Silvina de PinhoGarrahan Children’s Hospital, Buenos Aires, Argentina,
,
Fabiana LubienieckiGarrahan Children’s Hospital, Buenos Aires, Argentina,
,
Hugo A. ArroyoGarrahan Children’s Hospital, Buenos Aires, Argentina,
,
Marcela F. PereyraNotti Children’s Hospital, Mendoza, Argentina, and
,
Marcelo A. KauffmanJ.M. Ramos Mejía General Hospital, Buenos Aires, Argentina
&
María RoquéIHEM CCT-CONICET and National University of Cuyo, Mendoza, Argentina,
show all
Pages 2864-2867 | Received 07 Apr 2015, Accepted 17 May 2015, Published online: 26 Jun 2015

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Thanadon Dokrungkoon, Preyaporn Onsod, Prapatsorn Areesirisuk, Budsaba Rerkamnuaychoke, Kavin Vanikieti & Takol Chareonsirisuthigul. (2019) Performance of the MLPA technique for detecting common mutations in Leber hereditary optic neuropathy. Mitochondrial DNA Part A 30:8, pages 819-824.
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Lía Mayorga, Juan A. Cueto, Adriana P. Correa, María J. Guillamondegui, Mariana A. Loos, Verónica H. Araoz, Sergio R. Laurito & María Roqué. (2019) Maternally inherited Leigh syndrome detected by Multiplex ligation-dependent probe amplification. Mitochondrial DNA Part B 4:1, pages 530-533.
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Articles from other publishers (3)

Kristina Grigalionienė, Birutė Burnytė, Danutė Balkelienė, Laima Ambrozaitytė & Algirdas Utkus. (2022) Kearns‐Sayre syndrome case. Novel 5,9 kb mtDNA deletion . Molecular Genetics & Genomic Medicine 11:1.
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Mariana Amina Loos, Gimena Gomez, Lía Mayorga, Roberto Horacio Caraballo, Hernán Diego Eiroa, María Gabriela Obregon, Carlos Rugilo, Fabiana Lubieniecki, Ana Lía Taratuto, María Saccoliti, Cristina Noemi Alonso & Hilda Verónica Aráoz. (2021) Clinical and molecular characterization of mitochondrial DNA disorders in a group of Argentinian pediatric patients. Molecular Genetics and Metabolism Reports 27, pages 100733.
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J. K. Sofronova, Y. Y. Ilinsky, K. E. Orishchenko, E. G. Chupakhin, E. A. Lunev & I. O. Mazunin. (2016) Detection of mutations in mitochondrial DNA by droplet digital PCR. Biochemistry (Moscow) 81:10, pages 1031-1037.
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