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Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

PaperCitations, authors & open-access status

Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 136 citations, 2012 year and bronze oa status.

136
Citations
2012
Year
bronze
OA Status

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