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Molecular and clinical features of KATP‐channel neonatal diabetes mellitus in Japan

Molecular and clinical features of KATP‐channel neonatal diabetes mellitus in Japan

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1859738188

Molecular and clinical features of KATP‐channel neonatal diabetes mellitus in Japan

About this item

Full title

Molecular and clinical features of KATP‐channel neonatal diabetes mellitus in Japan

Publisher

Former Munksgaard: John Wiley & Sons A/S

Journal title

Pediatric diabetes, 2017-11, Vol.18 (7), p.532-539

Language

English

Formats

Publication information

Publisher

Former Munksgaard: John Wiley & Sons A/S

More information

Scope and Contents

Contents

Background
There are few reports pertaining to Asian patients with neonatal diabetes mellitus (NDM) caused by activating mutations in the ATP‐sensitive potassium channel genes (KATP‐NDM).
Objectives
To elucidate the characteristics of Japanese patients with KATP‐NDM.
Methods
By the amplification and direct sequencing of all exons and...

Alternative Titles

Full title

Molecular and clinical features of KATP‐channel neonatal diabetes mellitus in Japan

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1859738188

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1859738188

Other Identifiers

ISSN

1399-543X

E-ISSN

1399-5448

DOI

10.1111/pedi.12447

How to access this item