Title: Incidence and expression of the N1303K mutation of the cystic-fibrosis (CFTR) gene
Authors: Osborne, L ×
Santis, G
Schwarz, M
Klinger, K
Dork, T
Mcintosh, I
Schwartz, M
Nunes, V
Macek, M
Reiss, J
Highsmith, We
Mcmahon, R
Novelli, G
Malik, N
Burger, J
Anvret, M
Wallace, A
Williams, C
Mathew, C
Quarck, R
Graham, C
Gasparini, P
Balzarini, Jan
Cassiman, Jj
Balassopoulou, A
Davidow, L
Raskin, S
Kalaydjieva, L
Kerem, B
Richards, S
Simonbouy, B
Super, M
Wulbrand, U
Keston, M
Estivill, X
Vavrova, V
Friedman, Kj
Barton, D
Dallapiccola, B
Stuhrmann, M
Beards, F
Hill, Ajm
Pignatti, Pf
Cuppens, Harry
Angelicheva, D
Tummler, B
Brock, Djh
Casals, T
Macek, M
Schmidtke, J
Magee, Ac
Bonizzato, A
De Boeck, C
Kuffardjieva, A
Hodson, M
Knight, Ra #
Issue Date: Aug-1992
Publisher: Springer verlag
Series Title: Human Genetics vol:89 issue:6 pages:653-658
Abstract: The N1303K mutation was identified in the second nucleotide binding fold of the cystic fibrosis (CF) gene last year. We have gathered data from laboratories throughout Europe and the United States of America in order to estimate its frequency and to attempt to characterise the clinical manifestations of this mutation. N1303K, identified on 216 of nearly 15000 CF chromosomes tested, accounts for 1.5% of all CF chromosomes. The frequency of the N1303K allele varies significantly between countries and ethnic groups, being more common in Southern than in Northern Europe. This variation is independent of the DELTA-F508 allele. It was not found on UK Asian, American Black or Australian chromosomes. N1303K is associated with four different linked marker haplotypes for the polymorphic markers XV-2c, KM.19 and pMP6d-9. Ten patients are homozygous for this mutation, whereas 106 of the remainder carry one of 12 known CF mutations in the other CF allele. We classify N1303K as a "severe" mutation with respect to the pancreas, but can find no correlation between this mutation, in either the homozygous or heterozygous state, and the severity of lung disease.
ISSN: 0340-6717
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Human Mutations and Polymorphisms Section (-)
Laboratory of Virology and Chemotherapy (Rega Institute)
Department of Human Genetics - miscellaneous
× corresponding author
# (joint) last author

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