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Macular corneal dystrophy in a Chinese family related with novel mutations of CHST6

PURPOSE: To identify mutations in the carbohydrate sulfotransferase gene (CHST6) for a Chinese family with macular corneal dystrophy (MCD) and to investigate the histopathological changes in the affected cornea. METHODS: A corneal button of the proband was obtained by penetrating keratoplasty. The h...

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Detalhes bibliográficos
Main Authors: Dang, Xiuhong, Zhu, Qingguo, Wang, Li, Su, Hong, Lin, Hui, Zhou, Nan, Liang, Ting, Wang, Zheng, Huang, Shangzhi, Ren, Qiushi, Qi, Yanhua
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2666773/
https://ncbi.nlm.nih.gov/pubmed/19365571
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