The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype.
Saved in:
| Title: | The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype. |
|---|---|
| Authors: | Hamilton AJ; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, Devon, UK., Bingham C, McDonald TJ, Cook PR, Caswell RC, Weedon MN, Oram RA, Shields BM, Shepherd M, Inward CD, Hamilton-Shield JP, Kohlhase J, Ellard S, Hattersley AT |
| Source: | Journal of medical genetics [J Med Genet] 2014 Mar; Vol. 51 (3), pp. 165-9. Date of Electronic Publication: 2013 Nov 27. |
| Publication Type: | Case Reports; Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
Be the first to leave a comment!
