TY  - GEN
AU  - Yorifuji,Tohru
AU  - Kawakita,Rie
AU  - Nagai,Shizuyo
AU  - Sugimine,Akinori
AU  - Doi,Hiraku
AU  - Nomura,Anryu
AU  - Masue,Michiya
AU  - Nishibori,Hironori
AU  - Yoshizawa,Akihiko
AU  - Okamoto,Shinya
AU  - Doi,Ryuichiro
AU  - Uemoto,Shinji
AU  - Nagasaka,Hironori
TI  - Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes
SN  - 1945-7197
PY  - 2011///0204
KW  - Alleles
KW  - Asian People
KW  - genetics
KW  - Congenital Hyperinsulinism
KW  - DNA Mutational Analysis
KW  - Humans
KW  - Infant
KW  - KATP Channels
KW  - Microdissection
KW  - Mutation
KW  - Pancreatectomy
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1210/jc.2010-1281
ER  -