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...

Cur síos iomlán

Sonraí bibleagrafaíochta
Príomhchruthaitheoirí: Lombardo, Barbara, D'Argenio, Valeria, Monda, Emanuele, Vitale, Andrea, Caiazza, Martina, Sacchetti, Lucia, Pastore, Lucio, Limongelli, Giuseppe, Frisso, Giulia, Mazzaccara, Cristina
Formáid: Online Alt Téacs
Teanga:English
Foilsithe / Cruthaithe: John Wiley and Sons Inc. 2020
Ábhair:
Clinical Reports
Rochtain ar líne: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

Ar líne

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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