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.

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

doi:10.1136/jmg.2003.011890

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.

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

Norwich Medical School

Research output: Contribution to journal › Article › peer-review

65 Citations (Scopus)

Original language	English
Article number	e48
Journal	Journal of Medical Genetics
Volume	41
Issue number	4
DOIs	https://doi.org/10.1136/jmg.2003.011890
Publication status	Published - Apr 2004

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10.1136/jmg.2003.011890

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title = "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.",

author = "C. Mattocks and D. Baralle and P. Tarpey and C. ffrench-Constant and M. Bobrow and J. Whittaker",

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AU - Mattocks, C.

AU - Baralle, D.

AU - Tarpey, P.

AU - ffrench-Constant, C.

AU - Bobrow, M.

AU - Whittaker, J.

PY - 2004/4

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JF - Journal of Medical Genetics

IS - 4

M1 - e48

ER -

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.

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