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X-linked myxomatous valvular dystrophy in a patient with a novel mutation in the FLNA gene.
Madej-Pilarczyk, Agnieszka; Piekutowska-Abramczuk, Dorota; Kucinska, Beata; Furmanek, Mariusz; Gwiazda, Anna; Ciara, Elzbieta; Chrzanowska, Krystyna H; Werner, Bozena.
Affiliation
  • Madej-Pilarczyk A; Department of Medical Genetics, The Children's Memorial Health Institute, Warszawa, Poland. a.madej-pilarczyk@ipczd.pl.
  • Piekutowska-Abramczuk D; Department of Medical Genetics, The Children's Memorial Health Institute, Warszawa, Poland.
  • Kucinska B; Department of Pediatric Cardiology and General Pediatrics, Medical University of Warsaw, Warszawa, Poland.
  • Furmanek M; Department of Pediatric Radiology, Medical University of Warsaw, Warszawa, Poland.
  • Gwiazda A; Department of Pediatric Radiology, Medical University of Warsaw, Warszawa, Poland.
  • Ciara E; Department of Medical Genetics, The Children's Memorial Health Institute, Warszawa, Poland.
  • Chrzanowska KH; Department of Medical Genetics, The Children's Memorial Health Institute, Warszawa, Poland.
  • Werner B; Department of Pediatric Cardiology and General Pediatrics, Medical University of Warsaw, Warszawa, Poland.
Kardiol Pol ; 81(3): 306-307, 2023.
Article in En | MEDLINE | ID: mdl-36640296
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mitral Valve Prolapse / Genetic Diseases, X-Linked / Heart Defects, Congenital Limits: Humans Language: En Journal: Kardiol Pol Year: 2023 Document type: Article Affiliation country: Poland
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mitral Valve Prolapse / Genetic Diseases, X-Linked / Heart Defects, Congenital Limits: Humans Language: En Journal: Kardiol Pol Year: 2023 Document type: Article Affiliation country: Poland