The influence of rare genetic variation in SLC30A8 on diabetes incidence and β-Cell function

Authors

Liana K. Billings, Harvard Medical School
Kathleen A. Jablonski, George Washington UniversityFollow
Ronald T. Ackermann, Northwestern University
Andrew Taylor, Broad Institute, Cambridge, MA
Rebecca R. Fanelli, Massachusetts General Hospital, Boston, MA
+13 additional authors

Document Type

Journal Article

Publication Date

5-2014

Journal

Journal of Clinical Endocrinology and Metabolism

Volume

Volume 99, Issue 5

Inclusive Pages

E926-E930

Keywords

Cation Transport Proteins--genetics; Diabetes Mellitus, Type 2--genetics; Insulin-Secreting cells--secretion; Polymorphism--Single Nucleotide

Comments

This is an open access PubMed Central article. Click on link for full-text access.

APA Citation

Billings, L.K., Jablonski, K.A., Ackerman, R.J., Taylor, A., Fanelli, R.R. et al. (2014). The influence of rare genetic variation in SLC30A8 on diabetes incidence and β-Cell function. Journal of Clinical Endocrinology and Metabolism, 99(5), E926-E930.

Peer Reviewed

1

Open Access

1