Associated Papers
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.
Fujinami K et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2020
Association between Genetic Variations of MERTK and Chronic Obstructive Pulmonary Disease in Koreans.
Kim WJ et al.
Journal of Korean Medical Science, 2018
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