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Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patients Cover

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Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patients

Endocrine Regulations

Volume 52 (2018): Issue 2 (April 2018)

By: Daniel Danis, Katarina Brennerova, Martina Skopkova, Timea Kurdiova, Jozef Ukropec, Juraj Stanik, Miriam Kolnikova and Daniela Gasperikova

Open Access

|Apr 2018

Articles in this issue

DOI: https://doi.org/10.2478/enr-2018-0013 | Journal eISSN: 1336-0329 | Journal ISSN: 1210-0668

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Language: English

Page range: 110 - 118

Published on: Apr 30, 2018

Published by: Slovak Academy of Sciences, Institute of Experimental Endocrinology

In partnership with: Paradigm Publishing Services

Publication frequency: 1 issue per year

Keywords:

Leigh syndrome,

mitochondrial disease,

whole exome sequencing

Related subjects:

Molecular biology,

Basic medical science,

Basic medical science, other,

Clinical medicine,

Internal medicine,

Endocrinology, diabetology

© 2018 Daniel Danis, Katarina Brennerova, Martina Skopkova, Timea Kurdiova, Jozef Ukropec, Juraj Stanik, Miriam Kolnikova, Daniela Gasperikova, published by Slovak Academy of Sciences, Institute of Experimental Endocrinology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Volume 52 (2018): Issue 2 (April 2018)

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