Open Access UCL Research: Novel Heterozygous Deletion in Retinol Dehydrogenase 12 (RDH12) Causes Familial Autosomal Dominant Retinitis Pigmentosa. https://t.co/JQIEYYEkCT
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RT @MariyaMoosajee: Adding knowledge to the field, here’s our paper on novel heterozygous deletions in the retinol dehydrogenase 12 #RDH12…
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New Research: Novel Heterozygous Deletion in Retinol Dehydrogenase 12 (RDH12) Causes Familial Autosomal Dominant Retinitis Pigmentosa: Mutations in the retinol dehydrogenase 12 (RDH12) gene are primarily associated with Leber congenital… https://t.co/536nx
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RT @MariyaMoosajee: Adding knowledge to the field, here’s our paper on novel heterozygous deletions in the retinol dehydrogenase 12 #RDH12…