A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

INTRODUCTION: There are currently 23 missense point mutations and one 4 basepair deletion spanning different mitochondrial genes associated with mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS). The spectrum of mitochondrial DNA mutations in Arab patients with MELAS is...

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Detalles Bibliográficos
Autores principales: Abu-Amero, Khaled K, Al-Dhalaan, Hesham, Bohlega, Saeed, Hellani, Ali, Taylor, Robert W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Case report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2783076/
https://www.ncbi.nlm.nih.gov/pubmed/19946553
http://dx.doi.org/10.1186/1752-1947-3-77

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2783076/
https://www.ncbi.nlm.nih.gov/pubmed/19946553
http://dx.doi.org/10.1186/1752-1947-3-77

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