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Publications by Patrice Bouvagnet
A Systematic Variant Screening in Familial Cases of Congenital Heart Defects Demonstrates the Usefulness of Molecular Genetics in This Field
European Journal of Human Genetics
Genetics
Two Patients With the Heterozygous R189H Mutation in ACTA2 and Complex Congenital Heart Defects Expands the Cardiac Phenotype of Multisystemic Smooth Muscle Dysfunction Syndrome
American Journal of Medical Genetics, Part A
Genetics
A Novel Alpha Cardiac Actin (ACTC1) Mutation Mapping to a Domain in Close Contact With Myosin Heavy Chain Leads to a Variety of Congenital Heart Defects, Arrhythmia and Possibly Midline Defects
PLoS ONE
Multidisciplinary
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