Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: A boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutations-Reference-Cited by-同舟云学术

Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: A boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutations

Published:2004-02 Issue:2 Volume:70 Page:95-98
ISSN:1542-0752
Container-title:Birth Defects Research Part A: Clinical and Molecular Teratology
language:en
Short-container-title:Birth Defects Research Part A: Clinical and Molecular Teratology

Author:

Digilio M. Cristina,Pacileo Giuseppe,Sarkozy Anna,Limongelli Giuseppe,Conti Emanuela,Cerrato Fabiana,Marino Bruno,Pizzuti Antonio,Calabrò Raffaele,Dallapiccola Bruno

Funder

Italian Ministry of Health

Italian Ministry of Instruction, University and Research

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference20 articles.

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2. Phenotypic diversity in hypertrophic cardiomyopathy;Arad;Hum Mol Genet,2002

3. Missense mutation of the β-cardiac myosin heavy-chain gene in hypertrophic cardiomyopathy;Arai;Am J Med Genet,1995

4. Myocardial disarray in Noonan syndrome;Burch;Br Heart J,1992

5. Multiple lentigines syndrome (LEOPARD syndrome or progressive cardiomyopathic lentiginosis);Coppin;J Med Genet,1997

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