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Article

Identification of monogenic gene mutations in Japanese subjects diagnosed with type 1B diabetes between >5 and 15.1 years of age.

Journal of pediatric endocrinology & metabolism : JPEM - 1 Sept 2016

Moritani Maki, Yokota Ichiro, Horikawa Reiko, Urakami Tatsuhiko, Nishii Aki, Kawamura Tomoyuki, Kikuchi Nobuyuki, Kikuchi Touru, Ogata Tsutomu, Sugihara Shigetaka, Amemiya Shin

Abstract excerpt

BACKGROUND: Monogenic mutations, such as those in the potassium inwardly-rectifying channel, subfamily J, member 11 (KCNJ11) and insulin (INS) genes, are identified in young patients with type 1B diabetes (non-autoimmune-mediated). We recently reported the results of a test for monogenic forms of diabetes in Japanese children who were diagnosed with type 1B diabetes at <5 years of age. In this study, we tested...

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Source

Identifiers

PMID: 27398945
DOI: 10.1515/jpem-2016-0030

Genes

INS
KCNJ11

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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