Work

Molecular Analysis of Patients With Type III Bartter Syndrome: Picking Up Large Heterozygous Deletions With Semiquantitative PCR

Year: 2007

Type: article

Study design: Case Report

Source: Pediatric Research

DOI: 10.1203/pdr.0b013e318123fb90

Authors: Kandai Nozu, Xue Jun Fu, Koichi Nakanishi, Norishige Yoshikawa, Hiroshi Kaito, Kyoko Kanda, Rafal Przybyslaw Krol, Ritsuko Miyashita, Hidekazu Kamitsuji, Shoichiro Kanda, Yoshiki Hayashi, Kenichi Satomura, Nobuhiko Shimizu, Kazumoto Iijima, Masafumi Matsuo

Institutions: Kobe University, Wakayama Medical University, Ome Municipal General Hospital, Osaka Women's and Children's Hospital, National Center For Child Health and Development

Language: English

Topic: Ion Transport and Channel Regulation

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Ministry of Education, Culture, Sports, Science and Technology

OpenAlex ID: W1985305635

FWCI: 1.415

Cites: 20

Cited by: 48

Related to: 10