Cerebral arteriopathy associated with heterozygous Arg179Cys mutation in the ACTA2 gene: Report in 2 newborn siblings
José de Grazia(Vall d'Hebron Hospital Universitari), Élida Vázquez(Vall d'Hebron Hospital Universitari), Ignacio Delgado(Universitat Autònoma de Barcelona), Ángel Sánchez‐Montáñez(Vall d'Hebron Hospital Universitari), Susana Boronat(Vall d'Hebron Hospital Universitari), Miguel Del Campo(Vall d'Hebron Hospital Universitari)
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