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.

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.

UniProtKB (1)

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Mattocks C., Baralle D., Tarpey P., ffrench-Constant C., Bobrow M., Whittaker J.

J. Med. Genet. 41:E48-E48(2004) [PubMed] [Europe PMC]