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Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish.
Zahka, K; Kalidas, K; Simpson, M A; Cross, H; Keller, B B; Galambos, C; Gurtz, K; Patton, M A; Crosby, A H.
Affiliation
  • Zahka K; Department of Pediatrics, Division of Cardiology, Rainbow Babies and Children's Hospital, Case Western Reserve University, Cleveland, Ohio, USA.
Heart ; 94(10): 1326-30, 2008 Oct.
Article in En | MEDLINE | ID: mdl-18467358
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiomyopathy, Hypertrophic / Carrier Proteins / Protestantism / Homozygote / Mutation Type of study: Risk_factors_studies Limits: Female / Humans / Infant / Male Language: En Journal: Heart Journal subject: CARDIOLOGIA Year: 2008 Document type: Article Affiliation country: Estados Unidos Country of publication: Reino Unido
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiomyopathy, Hypertrophic / Carrier Proteins / Protestantism / Homozygote / Mutation Type of study: Risk_factors_studies Limits: Female / Humans / Infant / Male Language: En Journal: Heart Journal subject: CARDIOLOGIA Year: 2008 Document type: Article Affiliation country: Estados Unidos Country of publication: Reino Unido