Naoya Morisada
6PUBLICATIONS
4CO-AUTHORS
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Publications (6)
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|Sep 29, 2021
Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndrome.Nana Sakakibara, Takeshi Ijuin, Tomoko Horinouchi
|Sep 18, 2021
Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes.Shinya Ishiko, Naoya Morisada, Atsushi Kondo
|Apr 08, 2020
Bardet-Biedl syndrome in two unrelated patients with identical compound heterozygous SCLT1 mutations.Naoya Morisada, Riku Hamada, Kenichiro Miura
|May 28, 2019
Clinical characteristics of HNF1B-related disorders in a Japanese population.China Nagano, Naoya Morisada, Kandai Nozu
|Mar 13, 2016
Rare renal ciliopathies in non-consanguineous families that were identified by targeted resequencing.Tomohiko Yamamura, Naoya Morisada, Kandai Nozu
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