Identical intragenic microsatellite haplotype found in cystic fibrosis chromosomes bearing mutation G551D in Irish, English, Scottish, Breton and Czech patients.

S. M. Cashman,A. Patino,A. Martínez,M. García-Delgado,Z. Miedzybrodzka,Martin Schwarz,A. Shrimpton,Claude Férec,Odile Raguénès,Milan Macek,Nuria Morral,M. De Arce

Identical intragenic microsatellite haplotype found in cystic fibrosis chromosomes bearing mutation G551D in Irish, English, Scottish, Breton and Czech patients.

1995

S. M. Cashman
A. Patino
A. Martínez
M. García-Delgado
Z. Miedzybrodzka
Martin Schwarz
A. Shrimpton
Claude Férec
Odile Raguénès
Milan Macek
Nuria Morral
M. De Arce

Mutation G551D of exon 11 of the cystic fibrosis transmembrane conductance regulator gene is one of the most common mutations in patients of European origin. In order to test the hypothesis that the m

Keywords:

Cystic fibrosis
Microsatellite
Biology
Exon
Genetics
Haplotype
Mutation
Identity by descent
Mutation rate
Cystic fibrosis transmembrane conductance regulator
Pancreatic disease
Chromosome

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