Novel deletion mutation in the glucokinase gene from a korean man with GCK-MODY phenotype and situs inversus.

Abstract:

:A novel mutation in intron 9-exon 10 boundary of the GCK gene was detected in a male patient with clinical features of GCK-MODY and situs inversus. This case highlights the value of sequencing the GCK gene in individuals with GCK-MODY phenotype and no family history of monogenic diabetes.

authors

Cho YK,Cho EH,Choi HS,Kim SW

doi

10.1016/j.diabres.2018.07.036

subject

Has Abstract

pub_date

2018-09-01 00:00:00

pages

263-266

eissn

0168-8227

issn

1872-8227

pii

S0168-8227(18)30845-3

journal_volume

143

pub_type

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