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A novel mutation in the SERAC1 gene correlates with the severe manifestation of the MEGDEL phenotype, as revealed by whole-exome sequencing

The condition 3-methylglutaconic aciduria (3-MGA) with deafness, encephalopathy and Leigh-like (MEGDEL) syndrome, also known as 3-MGA IV, is one of a group of five rare metabolic disorders characterized by mitochondrial dysfunction, resulting in a series of phenotypic abnormalities. It is a rare, re...

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Dettagli Bibliografici
Pubblicato in:Exp Ther Med
Autori principali: Alagoz, Meryem, Kherad, Nasim, Turkmen, Selda, Bulut, Hatice, Yuksel, Adnan
Natura: Artigo
Lingua:Inglês
Pubblicazione: D.A. Spandidos 2020
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7185166/
https://ncbi.nlm.nih.gov/pubmed/32346411
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2020.8658
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