Advances in molecular genetic study on pathological myopia relevant gene loci / 中华实验眼科杂志
Chinese Journal of Experimental Ophthalmology
;
(12): 468-472, 2011.
Artigo
em Chinês
| WPRIM
| ID: wpr-635506
ABSTRACT
Pathological myopia(PM)is one of the global leading causes of blindness because of its severe optic complications.Previous researches implicated that hereditary factors play crucial roles in the pathogenesis of PM,and plenty molecular genetic studies,such as gene mapping and candidate gene screening,have been done to identify gene loci linked to PM.The newest advances in molecular genetic study on pathological myopia relevant gene loci were reviewed,including non-syndrome PM and system disease associated with PM.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Tipo de estudo:
Estudo prognóstico
Idioma:
Chinês
Revista:
Chinese Journal of Experimental Ophthalmology
Ano de publicação:
2011
Tipo de documento:
Artigo
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