Article

A novel homozygous Tub mutation associated with autosomal recessive retinitis pigmentosa in a consanguineous Chinese family

2022-05-31

Abstract excerpt

<title>Abstract</title> <bold>Background:</bold> Retinitis pigmentosa (RP) is the most common type of inherited retinopathy with at least 69 genes identified thus far. A significant proportion of RP, However, remains genetically unsolved. In this study, the the genetic basis of a Chinese consanguineous family with autosomal recessive retinitis pigmentosa (arRP) was investigated. <bold>Methods : </bold>Overall...

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Literature Corpus work: a996a1f1-f12c-540c-85f7-7e42ffc1b9d3
DOI: 10.21203/rs.3.rs-1678264/v1

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