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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Veröffentlicht in:Mol Vis
Hauptverfasser: Jinda, Worapoj, Poungvarin, Naravat, Taylor, Todd D., Suzuki, Yutaka, Thongnoppakhun, Wanna, Limwongse, Chanin, Lertrit, Patcharee, Suriyaphol, Prapat, Atchaneeyasakul, La-ongsri
Format: Artigo
Sprache:Inglês
Veröffentlicht: Molecular Vision 2016
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Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4842005/
https://ncbi.nlm.nih.gov/pubmed/27122965
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