Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domain.

Tools

Mattocks, C., Baralle, D., Tarpey, P., ffrench-Constant, C. ORCID: https://orcid.org/0000-0002-5621-3377, Bobrow, M. and Whittaker, J. (2004) Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domain. Journal of Medical Genetics, 41 (4). e48. ISSN 0022-2593

Full text not available from this repository. (Request a copy)

Item Type:	Article
Uncontrolled Keywords:	genetics,genetics(clinical) ,/dk/atira/pure/subjectarea/asjc/1300/1311
Faculty \ School:	Faculty of Medicine and Health Sciences > Norwich Medical School
Related URLs:	http://www.scopus.com/inward/record.url?...
Depositing User:	LivePure Connector
Date Deposited:	16 Jul 2022 12:30
Last Modified:	23 Oct 2022 03:57
URI:	https://ueaeprints.uea.ac.uk/id/eprint/86340
DOI:	10.1136/jmg.2003.011890

Actions (login required)

View Item