Cargando…
Molecular analysis of the choroideremia gene related clinical findings in two families with choroideremia
PURPOSE: To investigate the choroideremia (CHM) gene in two families with CHM and to characterize the related clinical features. METHODS: Two families underwent complete ophthalmic examinations and three males were diagnosed with CHM. Genomic DNA was extracted from the leukocytes of peripheral blood...
Autores principales: | Lin, Ying, Liu, Xialin, Luo, Lixia, Qu, Bo, Jiang, Shuhong, Yang, Huiqin, Liang, Xuanwei, Ye, Shaobi, Liu, Yizhi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198496/ https://www.ncbi.nlm.nih.gov/pubmed/22025891 |
Ejemplares similares
-
A Case Study of Choroideremia and Choroideremia Carrier
por: Pidro, Ajla, et al.
Publicado: (2019) -
Molecular Therapies for Choroideremia
por: Cehajic Kapetanovic, Jasmina, et al.
Publicado: (2019) -
Choroideremia Gene Therapy
por: Lam, Byron L., et al.
Publicado: (2021) -
Choroideremia: The Endpoint Endgame
por: Abdalla Elsayed, Maram E. A., et al.
Publicado: (2023) -
FGFR2 molecular analysis and related clinical findings in one Chinese family with Crouzon Syndrome
por: Lin, Ying, et al.
Publicado: (2012)