Publication | Open Access
Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly
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Citations
41
References
2009
Year
CardiomyopathyMolecular PhysiologyGenetic DisorderGeneticsHuman Heart DefectsNodal MutationsCongenital Heart DefectCongenital Heart AnomalyMedicineCell BiologyCell SignalingCumulative Ligand Activity
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