A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness, identifies the gene for Usher syndrome type 1C Meeting Abstract
| Authors: | Bitner-Glindzicz, M.; Rutland, P.; Lindley, K. J.; Blaydon, D.; Smith, V. V.; Milla, P. J.; Hussain, K.; Furth-Lavi, J.; Cosgrove, K. E.; Shepherd, R. M.; Barnes, P. D.; O'Brien, R. E.; Sowden, J.; Scanlan, M. J.; Malcolm, S.; Dunne, M. J.; Aynsley-Green, A.; Glaser, B. |
| Abstract Title: | A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness, identifies the gene for Usher syndrome type 1C |
| Meeting Title: | 50th Annual Meeting of the American Society of Human Genetics (ASHG) |
| Journal Title: | American Journal of Human Genetics |
| Volume: | 67 |
| Issue: | 4 Suppl. 2 |
| Meeting Dates: | 2000 Oct 3-7 |
| Meeting Location: | Philadelphia, PA |
| ISSN: | 0002-9297 |
| Publisher: | Cell Press |
| Date Published: | 2000-10-01 |
| Start Page: | 41 |
| Language: | English |
| ACCESSION: | WOS:000089400700151 |
| PROVIDER: | wos |
| PUBMED: | 11028187 |
| Notes: | Meeting Abstract: 148 -- Source: Wos |
