Skip to Main Content

Skip Nav Destination

Abstract| March 01 2000

A severe clinical phenotype results from the co-inheritance of type 2 susceptibility genes and a hepatocyte nuclear factor-1alpha mutation.

C J Tack;

C J Tack

Search for other works by this author on:

PubMed

Google Scholar

S Ellard;

S Ellard

Search for other works by this author on:

PubMed

Google Scholar

A T Hattersley

A T Hattersley

Search for other works by this author on:

PubMed

Google Scholar

Diabetes Care 2000;23(3):424–425

https://doi.org/10.2337/diacare.23.3.424

PubMed:

10868881