Literature DB >> 18676185

Three novel mutations in the CFTR gene identified in Galician patients.

P Rana-Díez1, C Colón, J R Alonso-Fernández, A Solar, J C Barros-Tizón, D Barros-Casas, J Sirvent, A Carracedo, F Barros.   

Abstract

We report three novel CFTR missense mutations detected in Spanish patients from Galicia (North West of Spain). In the first case, a patient homozygous for a novel S1045Y mutation died due to pulmonary problems. In the other two cases, both heterozygous for novel mutations combined with the F508del mutation, clinical symptoms were different depending on the mutation, detected as M595I and A107V.

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Year:  2008        PMID: 18676185     DOI: 10.1016/j.jcf.2008.05.009

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  3 in total

1.  Description of rare mutations and a novel variant in Brazilian patients with Cystic Fibrosis: a case series from a referral center in the Bahia State.

Authors:  Laís Ribeiro Mota; Valmir Machado de Melo Filho; Lorena Lemos de Castro; Daniel Fantozzi Garcia; Regina Terse-Ramos; Maria Betânia Pereira Toralles; Renata Lúcia Leite Ferreira de Lima; Edna Lúcia Souza
Journal:  Mol Biol Rep       Date:  2018-09-19       Impact factor: 2.316

Review 2.  Personalized medicine in CF: from modulator development to therapy for cystic fibrosis patients with rare CFTR mutations.

Authors:  Misak Harutyunyan; Yunjie Huang; Kyu-Shik Mun; Fanmuyi Yang; Kavisha Arora; Anjaparavanda P Naren
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2017-12-14       Impact factor: 5.464

3.  Personalized medicine in cystic fibrosis: genistein supplementation as a treatment option for patients with a rare S1045Y-CFTR mutation.

Authors:  Kavisha Arora; Sunitha Yarlagadda; Weiqiang Zhang; ChangSuk Moon; Erin Bouquet; Saumini Srinivasan; Chunying Li; Dennis C Stokes; Anjaparavanda P Naren
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2016-06-03       Impact factor: 5.464

  3 in total

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