Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
December 8, 2008Human Molecular GeneticsOpen Access

Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations

View Full Paper
Ask AI
Bookmark
Share

Authors

BMBhagyalaxmi MohapatraThe University of Texas MD Anderson Cancer CenterBCBrett CaseyChildren's & Women's Health Centre of British ColumbiaHLHua LiUniversity of California, San Francisco

Discussion

Loading...

Member takes

Overview

Key Points

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

Cite This Study

Mohapatra et al. (2008) studied this question.

synapsesocial.com/papers/6a85739d02a1bc3ea31e5bedhttps://doi.org/10.1093/hmg/ddn411
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1The transcription factor FoxH1 (FAST) mediates Nodal signaling during anterior-posterior patterning and node formation in the mouse2001 · 223 citations
  2. 2Left-right axis malformations associated with mutations inACVR2B, the gene for human activin receptor type IIB1999 · 201 citations