INSTITUTION'S PROFILE

Department of Genome Medicine, National Center for Child Health and Development, Tokyo, Japan.

Publications (1)

Renal coloboma syndrome/dominant optic atrophy with severe retinal atrophy and de novo digenic mutations in PAX2 and OPA1.

Journal: Pediatric nephrology (Berlin, Germany)

Publication date: 

Journal: Pediatric nephrology (Berlin, Germany)

Publication Year: 

Authors & Co-authors:  Shimabukuro Chinen Imanaga Yanagi Kaname Nakanishi