Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
September 1, 2004Journal of Medical GeneticsOpen Access

Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease

View Full Paper
Ask AI
Bookmark
Share

Authors

SRStella Marie Reamon-BuettnerFraunhofer Institute for Toxicology and Experimental Medicine

Discussion

Loading...

Member takes

Overview

Key Points

Key points are not available for this paper at this time.

Cite This Study

Stella Marie Reamon-Buettner (2004) studied this question.

synapsesocial.com/papers/6aa29d774353e7526aa89a24https://doi.org/10.1136/jmg.2003.017483
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1NKX2.5 Mutations in Patients With Tetralogy of Fallot2001 · 344 citations
  2. 2Multiple mutations and cancer2003 · 762 citations
  3. 3Progressive AV-block and anomalous venous return among cardiac anomalies associated with two novel missense mutations in theCSX/NKX2-5 Gene2002 · 77 citations