Molecular and Clinical Analysis of Japanese Patients with Persistent Congenital Hyperinsulinism: Predominance of Paternally Inherited Monoallelic Mutations in the K<sub>ATP</sub>Channel Genes - Concepedia

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Molecular and Clinical Analysis of Japanese Patients with Persistent Congenital Hyperinsulinism: Predominance of Paternally Inherited Monoallelic Mutations in the K<sub>ATP</sub>Channel Genes

DOI Full Paper Access

42

Citations

16

References

2010

Year

Tohru Yorifuji, Rie Kawakita, Shizuyo Nagai, Akinori Sugimine, Hiraku Doi, Anryu Nomura, Michiya Masue, Hironori Nishibori, Akihiko Yoshizawa, Shinya Okamoto,

The Journal of Clinical Endocrinology & Metabolism

Abstract

The majority of the Japanese patients with K(ATP) channel hyperinsulinism (84.2%) demonstrated paternally inherited monoallelic mutations that accurately predicted the presence of the focal form.

References

	Year	Citations

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