A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa

PURPOSE: Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous group of inherited retinal degenerations characterized by progressive loss of photoreceptor cells and RPE functions. More than 70 causative genes are known to be responsible for RP. This study aimed to identify the caus...

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Detalles Bibliográficos
Publicado en:Mol Vis
Main Authors: Jinda, Worapoj, Poungvarin, Naravat, Taylor, Todd D., Suzuki, Yutaka, Thongnoppakhun, Wanna, Limwongse, Chanin, Lertrit, Patcharee, Suriyaphol, Prapat, Atchaneeyasakul, La-ongsri
Formato: Artigo
Idioma:Inglês
Publicado: Molecular Vision 2016
Assuntos:
Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4842005/
https://ncbi.nlm.nih.gov/pubmed/27122965
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