Open AccessNext-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment
Author(s) -
Meriem Hechmi,
Majida Charif,
Ichraf Kraoua,
Meriem Fassatoui,
Hamza Dallali,
Valérie DesquiretDumas,
Céline Bris,
David Goudenège,
C. Drissi,
Saïd Galaï,
Slah Ouerhani,
Vincent Procaccio,
Patrizia AmatiBonneau,
Sonia Abdelhak,
Ilhem Ben Youssef-Turki,
Guy Lenaers,
Rym Kéfi
Publication year - 2022
Publication title -
bioscience reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.938
H-Index - 77
eISSN - 1573-4935
pISSN - 0144-8463
DOI - 10.1042/bsr20220194
Subject(s) - mitochondrial dna , thiamine , genetics , leigh disease , gene , biology , nuclear gene , dna sequencing , mitochondrial disease , mitochondrion , genome , microbiology and biotechnology , biochemistry
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