Literature DB >> 7666889

Connexin43 mutations in sporadic and familial defects of laterality.

B Casey, A Ballabio.   

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Year:  1995        PMID： 7666889     DOI： 10.1056/NEJM199510053331415

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  3 in total

1.  Absence of mutations in the regulatory domain of the gap junction protein connexin 43 in patients with visceroatrial heterotaxy.

Authors:  M Penman Splitt; M Y Tsai; J Burn; J A Goodship
Journal:  Heart       Date:  1997-04       Impact factor: 5.994

2.  Spectrum of Genetic Variants in a Cohort of 37 Laterality Defect Cases.

Authors:  Dinu Antony; Elif Gulec Yilmaz; Alper Gezdirici; Lennart Slagter; Zeineb Bakey; Helen Bornaun; Ibrahim Cansaran Tanidir; Tran Van Dinh; Han G Brunner; Peter Walentek; Sebastian J Arnold; Rolf Backofen; Miriam Schmidts
Journal:  Front Genet       Date:  2022-04-13       Impact factor: 4.772

3.  Connexin26-mediated transfer of laterality cues in Xenopus.

Authors:  Tina Beyer; Thomas Thumberger; Axel Schweickert; Martin Blum
Journal:  Biol Open       Date:  2012-03-30       Impact factor: 2.422
  3 in total

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