Literature DB >> 7691349

Severe splice site mutation preceding exon 9 of the CFTR gene.

T Dörk1, R Fislage, U Rappen, B Tümmler.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1993        PMID： 7691349     DOI： 10.1093/hmg/2.8.1313

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


× No keyword cloud information.
  3 in total

1.  Geographic distribution and origin of CFTR mutations in Germany.

Authors:  B Tümmler; T Storrs; V Dziadek; T Dörk; T Meitinger; A Golla; R M Bertele-Harms; H K Harms; E Schröder; A Claass; J Rutjes; R Schneppenheim; I Bauer; K Breuel; M Stuhrmann; J Schmidtke; M Lindner; A Eigel; J Horst; R Kaiser; M J Lentze; K Schmidt; H von der Hardt; X Estivill
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

2.  Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutations.

Authors:  T Dörk; R Fislage; T Neumann; B Wulf; B Tümmler
Journal:  Hum Genet       Date:  1994-01       Impact factor: 4.132

3.  Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients.

Authors:  T Dörk; F Mekus; K Schmidt; J Bosshammer; R Fislage; T Heuer; V Dziadek; T Neumann; N Kälin; U Wulbrand
Journal:  Hum Genet       Date:  1994-11       Impact factor: 4.132
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.