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A Familial Congenital Heart Disease with a Possible Multigenic Origin Involving a Mutation in BMPR1A
A Familial Congenital Heart Disease with a Possible Multigenic Origin Involving a Mutation in BMPR1A
2019
J. T. Demal
M. Heise
Benedikt Reiz
Deepika Dogra
Ingrid Brænne
Hermann Reichenspurner
Jörg Männer
Zouhair Aherrahrou
Heribert Schunkert
Jeanette Erdmann
Salim Abdelilah-Seyfried
Keywords:
Intensive care medicine
BMPR1A
Pediatrics
Heart disease
Medicine
Mutation
Correction
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