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UnknownPanel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies.
Not available
S-EPMC3865404 | biostudies-literature
UnknownClinical Phenotype of PDE6B-Associated Retinitis Pigmentosa.
Not available
S-EPMC7956818 | biostudies-literature
UnknownTRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
Not available
S-EPMC2775830 | biostudies-literature
UnknownClinical Phenotype and Course of PDE6A-Associated Retinitis Pigmentosa Disease, Characterized in Preparation for a Gene Supplementation Trial.
Not available
S-EPMC7563671 | biostudies-literature
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