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Published in 2022 at "Genes"
DOI: 10.3390/genes13050925
Abstract: The retinal dystrophy phenotype associated with CDHR1 retinopathy is clinically heterogenous. In this study, we describe the clinical and molecular findings of a retinal dystrophy cohort (10 patients) attributed to autosomal recessive CDHR1 and report…
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Keywords:
cdhr1 associated;
dystrophy;
phenotypes cdhr1;
clinical phenotypes ... See more keywords