Interpretation of genetic variants depends on a clinically guided integration of phenotype and molecular data.

Arbustini, Eloisa; Urtis, Mario; Elliott, Perry

Arbustini, Eloisa; Urtis, Mario; Elliott, Perry.

Afiliação

Arbustini E; Transplant Research Area and Centre for Inherited Cardiovascular Diseases, Department of Medical Sciences and Infectious Diseases, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Urtis M; Transplant Research Area and Centre for Inherited Cardiovascular Diseases, Department of Medical Sciences and Infectious Diseases, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Elliott P; Department of Inherited cardiovascular diseases, Barts Heart Centre St Bartholomew's Hospital, London, UK.

Eur Heart J ; 43(27): 2638-2639, 2022 07 14.

Article em En | MEDLINE | ID: mdl-35598036

Assuntos

Cardiologia; Cardiomiopatias; Genética Médica; Consenso; Genômica; Humanos; Fenótipo

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cardiologia / Genética Médica / Cardiomiopatias Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: Eur Heart J Ano de publicação: 2022 Tipo de documento: Article

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