Search details
1.
Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy.
BMC Med Genet
; 11: 67, 2010 Apr 30.
Article
in English
| MEDLINE | ID: mdl-20433692
2.
Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.
Hum Genet
; 127(4): 483, 2010 Apr.
Article
in English
| MEDLINE | ID: mdl-21488259
3.
Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.
Hum Genet
; 127(4): 484, 2010 Apr.
Article
in English
| MEDLINE | ID: mdl-21488307
4.
Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.
Hum Genet
; 127(4): 483, 2010 Apr.
Article
in English
| MEDLINE | ID: mdl-21488306
5.
Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.
Hum Genet
; 127(4): 484, 2010 Apr.
Article
in English
| MEDLINE | ID: mdl-21488308
6.
Phenotype and prognostic correlations of the converter region mutations affecting the ß myosin heavy chain.
Heart
; 101(13): 1047-53, 2015 Jul.
Article
in English
| MEDLINE | ID: mdl-25935763
7.
A homozygous MYBPC3 gene mutation associated with a severe phenotype and a high risk of sudden death in a family with hypertrophic cardiomyopathy.
Rev Esp Cardiol
; 62(5): 572-5, 2009 May.
Article
in English, Spanish
| MEDLINE | ID: mdl-19406073
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