Case Reports
[Familial hypertrophic cardiomyopathy--a case report]
[Article in
Polish]
Affiliations
- PMID: 17165166
Item in Clipboard
Case Reports
[Familial hypertrophic cardiomyopathy--a case report]
[Article in
Polish]
Kardiol Pol.
2006 Nov.
Abstract
Genetic profile od four-generation family with hypertrophic cardiomyopathy is presented. The alterations in the MYH7 gene sequences were identified. Genetic background of familial hypertrophic cardiomyopathy is reviewed and discussed.
Similar articles
-
One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region.Eur J Hum Genet. 2005 Feb;13(2):161-5. doi: 10.1038/sj.ejhg.5201310. Eur J Hum Genet. 2005. PMID: 15483641
-
Denaturing high performance liquid chromatography: high throughput mutation screening in familial hypertrophic cardiomyopathy and SNP genotyping in motor neurone disease.J Clin Pathol. 2005 May;58(5):479-85. doi: 10.1136/jcp.2004.021642. J Clin Pathol. 2005. PMID: 15858117 Free PMC article.
-
Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations.Cardiovasc Res. 2003 Feb;57(2):347-57. doi: 10.1016/s0008-6363(02)00711-3. Cardiovasc Res. 2003. PMID: 12566107
-
A contemporary approach to hypertrophic cardiomyopathy.Circulation. 2006 Jun 20;113(24):e858-62. doi: 10.1161/CIRCULATIONAHA.105.591982. Circulation. 2006. PMID: 16785342 Review. No abstract available.
-
Familial hypertrophic cardiomyopathy: clinical features, molecular genetics and molecular genetic testing.Expert Rev Mol Diagn. 2004 Jan;4(1):99-113. doi: 10.1586/14737159.4.1.99. Expert Rev Mol Diagn. 2004. PMID: 14711353 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Molecular Biology Databases