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4. CEP78 is mutated in a distinct type of Usher syndrome. Issue 3 (14th September 2016)

6. Clinical and genetic characteristics of 10 Japanese patients with PROM1‐associated retinal disorder: A report of the phenotype spectrum and a literature review in the Japanese population. Issue 3 (20th August 2020)

7. Clinical and genetic characteristics of Stargardt disease in a large Western China cohort: Report 1. Issue 3 (26th August 2020)