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Article

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 - 1 Apr 2004

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

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Share to DNA Mutational Analysis
Share to Exons
Share to Genes, Neurofibromatosis 1
Share to GTPase-Activating Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Neurofibromatosis 1

Share to Neurofibromin 1

Share to Polymorphism, Genetic

Share to Protein Structure, Tertiary

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Identifiers

PMID: 15060124
DOI: 10.1136/jmg.2003.011890
PMCID: PMC1735749

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