The clinical implications of molecular monitoring and analyses of inherited retinal diseases
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DOI: 10.1080/14737159.2017.1384314
Abstract: ABSTRACT Introduction: Retinal dystrophies (RDs) are the most common cause of inherited blindness and one of the most genetically heterogeneous human diseases. RDs arise from mutations in genes involved in development and function of photoreceptors… read more here.
Keywords: monitoring analyses; molecular monitoring; diagnosis; clinical implications ... See more keywords