A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment

Mitochondrial complex III deficiency nuclear type 2 is an autosomal-recessive disorder caused by mutations in TTC19 gene. TTC19 is involved in the preservation of mitochondrial complex III, which is responsible for transfer of electrons from reduced coenzyme Q to cytochrome C and thus, contributes t...

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Detalles Bibliográficos
Autores principales: Habibzadeh, Parham, Inaloo, Soroor, Silawi, Mohammad, Dastsooz, Hassan, Farazi Fard, Mohammad Ali, Sadeghipour, Forough, Faghihi, Zahra, Rezaeian, Mohaddeseh, Yavarian, Majid, Böhm, Johann, Faghihi, Mohammad Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737916/
https://www.ncbi.nlm.nih.gov/pubmed/31551910
http://dx.doi.org/10.3389/fneur.2019.00944

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737916/
https://www.ncbi.nlm.nih.gov/pubmed/31551910
http://dx.doi.org/10.3389/fneur.2019.00944

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