Items where Author is "Imagawa, E."

Article

(2016) A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract. Journal of Human Genetics. pp. 177-179. ISSN 1434-5161

(2015) Two novel homozygous RAB3GAP1 mutations cause Warburg micro syndrome. Human genome variation. p. 15034. ISSN 2054-345X (Print) 2054-345X (Linking)