Progress in molecular Biology of MELAS / 基础医学与临床
Basic & Clinical Medicine
;
(12)2006.
Artículo
en Chino
| WPRIM
| ID: wpr-594195
ABSTRACT
MELAS syndrome(mitochondrial myopathy encephalophathy with lactic acidosis and stroke-like episodes),as one of the most common diseases in mitochondrial encephalomyopathies,is characterized by highly variable manifestations.So,more and more people come to realize the importance of molecular basis of MELAS.This review took the commonest mtDNA point mutation(A3243G) for example to overview its molecular biological mechanism,test strategy and recent progress of study on MELAS syndrome.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Idioma:
Chino
Revista:
Basic & Clinical Medicine
Año:
2006
Tipo del documento:
Artículo
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