Glucokinase Gene Mutations Are Not a Common Cause of Permanent Neonatal Diabetes in France

Diabetologia - Germany
doi 10.1007/s00125-001-0741-1
Full Text
Abstract

Available in full text

Date
Authors

Unknown

Publisher

Springer Science and Business Media LLC

Related search

A New Compound Heterozygosis for Inactivating Mutations in the Glucokinase Gene as Cause of Permanent Neonatal Diabetes Mellitus (PNDM) in Double-First Cousins

Diabetology and Metabolic Syndrome
Internal MedicineEndocrinologyMetabolismDiabetes
2015English

SMARCB1 Mutations Are Not a Common Cause of Multiple Meningiomas

Journal of Medical Genetics
Genetics
2010English

Trisomy 21 Is a Cause of Permanent Neonatal Diabetes That Is Autoimmune but Not HLA Associated

Diabetes
Internal MedicineEndocrinologyMetabolismDiabetes
2019English

Trisomy 21 Is a Cause of Permanent Neonatal Diabetes That Is Autoimmune but Not HLA Associated

Yearbook of Paediatric Endocrinology
2019English

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes

Diabetes
Internal MedicineEndocrinologyMetabolismDiabetes
2017English

Permanent Neonatal Diabetes Mellitus

2020English

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes

Yearbook of Paediatric Endocrinology
2018English

PIK3CA Mutations Are Common in Lobular Carcinoma in Situ, but Are Not a Biomarker of Progression

Breast Cancer Research
Cancer ResearchOncology
2017English

Common Polymorphisms in the Adiponectin Gene ACDC Are Not Associated With Diabetes in Pima Indians

Diabetes
Internal MedicineEndocrinologyMetabolismDiabetes
2004English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy