A rare case of pediatric cardiomyopathy: Alström syndrome identified by gene panel analysis
A rare case of pediatric cardiomyopathy: Alström syndrome identified by gene panel analysis
About this item
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Author / Creator
Publisher
England: John Wiley & Sons, Inc
Journal title
Language
English
Formats
Publication information
Publisher
England: John Wiley & Sons, Inc
Subjects
More information
Scope and Contents
Contents
Genetic investigation of early‐onset Dilatative cardiomyopathy phenotype, including molecular autopsy, is the key to appropriate recognition and management of rare etiologies and atypical presentations and to offer genetic counseling to the family.
Genetic investigation of early‐onset Dilatative cardiomyopathy phenotype, including molecular auto...
Alternative Titles
Full title
A rare case of pediatric cardiomyopathy: Alström syndrome identified by gene panel analysis
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Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_a1839f6f9f5b438fa2629f0563cfa98f
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a1839f6f9f5b438fa2629f0563cfa98f
Other Identifiers
ISSN
2050-0904
E-ISSN
2050-0904
DOI
10.1002/ccr3.3327
