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Leigh Syndrome in a Pedigree Harboring the m.1555A>G Mutati..:
Mouna Habbane
;
Laura Llobet
;
M. Pilar Bayona-Bafaluy
...
Human Genomics and Genetic Diseases. , 2020
Link:
https://doi.org/10.3390/genes11091007
RT Journal T1
Leigh Syndrome in a Pedigree Harboring the m.1555A>G Mutation in the Mitochondrial 12S rRNA
UL https://suche.suub.uni-bremen.de/peid=base-ftmdpi:oai:mdpi.com:_2073-4425_11_9_1007_&Exemplar=1&LAN=DE A1 Mouna Habbane A1 Laura Llobet A1 M. Pilar Bayona-Bafaluy A1 José E. Bárcena A1 Leticia Ceberio A1 Covadonga Gómez-Díaz A1 Laura Gort A1 Rafael Artuch A1 Julio Montoya A1 Eduardo Ruiz-Pesini PB Multidisciplinary Digital Publishing Institute YR 2020 K1 Leigh syndrome K1 hearing loss K1 mitochondrial DNA K1 ribosomal RNA K1 pathologic mutation K1 penetrance JF Human Genomics and Genetic Diseases LK http://dx.doi.org/https://doi.org/10.3390/genes11091007 DO https://doi.org/10.3390/genes11091007 SF ELIB - SuUB Bremen
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