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You searched for: Author/Creator Yang, Lisha

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1. A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree. Issue 5 (20th March 2019)

2. A novel, homozygous nonsense variant of the CDHR1 gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS‐based genetic diagnosis. Issue 11 (30th August 2018)