Myofibrillar Cardiomyopathy due to a Novel Desmin Gene Mutation: Complementary Role of Echocardiography, Cardiac Magnetic Resonance, and Genetic Testing in Delineating Diagnosis.

Koitka, Karen; Dahiya, Arun; Lo, Ada; Scalia, Gregory M; Atherton, John J; Prasad, Sandhir B

Koitka, Karen; Dahiya, Arun; Lo, Ada; Scalia, Gregory M; Atherton, John J; Prasad, Sandhir B.

Afiliación

Koitka K; Cardiology Department, Royal Brisbane and Women's Hospital, Brisbane, Australia.
Dahiya A; Cardiology Department, Royal Brisbane and Women's Hospital, Brisbane, Australia.
Lo A; Cardiology Department, Royal Brisbane and Women's Hospital, Brisbane, Australia.
Scalia GM; Cardiology Department, The Prince Charles Hospital, Brisbane, Australia.
Atherton JJ; Cardiology Department, Royal Brisbane and Women's Hospital, Brisbane, Australia.
Prasad SB; Cardiology Department, Royal Brisbane and Women's Hospital, Brisbane, Australia.

CASE (Phila) ; 1(1): 28-33, 2017 Feb.

Article en En | MEDLINE | ID: mdl-30062237

Palabras clave

Desminopathy; Myofibrillar cardiomyopathy

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: CASE (Phila) Año: 2017 Tipo del documento: Article País de afiliación: Australia

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