Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndrome

BACKGROUND: Syndromic dilated cardiomyopathy (DCM) includes a group of complex disorders with a very heterogeneous genetic etiology, leading to delay in definitive diagnosis. Conversely, an early genetic diagnosis is very important in determining the disease course, the prognosis, and may guide pers...

Szczegółowa specyfikacja

Opis bibliograficzny
Główni autorzy: Lombardo, Barbara, D'Argenio, Valeria, Monda, Emanuele, Vitale, Andrea, Caiazza, Martina, Sacchetti, Lucia, Pastore, Lucio, Limongelli, Giuseppe, Frisso, Giulia, Mazzaccara, Cristina
Format: Online Artykuł Texto
Język:English
Wydane: John Wiley and Sons Inc. 2020
Hasła przedmiotowe:
Clinical Reports
Dostęp online:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336746/
https://www.ncbi.nlm.nih.gov/pubmed/32396277
http://dx.doi.org/10.1002/mgg3.1260

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336746/
https://www.ncbi.nlm.nih.gov/pubmed/32396277
http://dx.doi.org/10.1002/mgg3.1260

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