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.

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

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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
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Depositing User: LivePure Connector
Date Deposited: 16 Jul 2022 12:30
Last Modified: 21 Jul 2022 08:32
URI: https://ueaeprints.uea.ac.uk/id/eprint/86340
DOI: 10.1136/jmg.2003.011890

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