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Familial hypertrophic cardiomyopathy associated with a new mutation in gene MYBPC3
We think that the main interests of this study are the report of a new mutation in gene MYBPC3 as a cause of Hypertrophic cardiomyopathy (HMC), and the verification of the fact that not always is the number of mutations related to the severity of the disease.
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331257/ https://www.ncbi.nlm.nih.gov/pubmed/28265379 http://dx.doi.org/10.1002/ccr3.832 |
| _version_ | 1782511336980217856 |
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| author | Aurensanz Clemente, Esther Ayerza Casas, Ariadna García Lasheras, Cecilia Ramos Fuentes, Feliciano Bueno Martínez, Ines Pelegrín Díaz, Juana Ruiz Frontera, Pablo Montserrat Iglesias, Lorenzo |
| author_facet | Aurensanz Clemente, Esther Ayerza Casas, Ariadna García Lasheras, Cecilia Ramos Fuentes, Feliciano Bueno Martínez, Ines Pelegrín Díaz, Juana Ruiz Frontera, Pablo Montserrat Iglesias, Lorenzo |
| author_sort | Aurensanz Clemente, Esther |
| collection | PubMed |
| description | We think that the main interests of this study are the report of a new mutation in gene MYBPC3 as a cause of Hypertrophic cardiomyopathy (HMC), and the verification of the fact that not always is the number of mutations related to the severity of the disease. |
| format | Online Article Text |
| id | pubmed-5331257 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2017 |
| publisher | John Wiley and Sons Inc. |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-53312572017-03-06 Familial hypertrophic cardiomyopathy associated with a new mutation in gene MYBPC3 Aurensanz Clemente, Esther Ayerza Casas, Ariadna García Lasheras, Cecilia Ramos Fuentes, Feliciano Bueno Martínez, Ines Pelegrín Díaz, Juana Ruiz Frontera, Pablo Montserrat Iglesias, Lorenzo Clin Case Rep Case Reports We think that the main interests of this study are the report of a new mutation in gene MYBPC3 as a cause of Hypertrophic cardiomyopathy (HMC), and the verification of the fact that not always is the number of mutations related to the severity of the disease. John Wiley and Sons Inc. 2017-01-27 /pmc/articles/PMC5331257/ /pubmed/28265379 http://dx.doi.org/10.1002/ccr3.832 Text en © 2017 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
| spellingShingle | Case Reports Aurensanz Clemente, Esther Ayerza Casas, Ariadna García Lasheras, Cecilia Ramos Fuentes, Feliciano Bueno Martínez, Ines Pelegrín Díaz, Juana Ruiz Frontera, Pablo Montserrat Iglesias, Lorenzo Familial hypertrophic cardiomyopathy associated with a new mutation in gene MYBPC3 |
| title | Familial hypertrophic cardiomyopathy associated with a new mutation in gene MYBPC3 |
| title_full | Familial hypertrophic cardiomyopathy associated with a new mutation in gene MYBPC3 |
| title_fullStr | Familial hypertrophic cardiomyopathy associated with a new mutation in gene MYBPC3 |
| title_full_unstemmed | Familial hypertrophic cardiomyopathy associated with a new mutation in gene MYBPC3 |
| title_short | Familial hypertrophic cardiomyopathy associated with a new mutation in gene MYBPC3 |
| title_sort | familial hypertrophic cardiomyopathy associated with a new mutation in gene mybpc3 |
| topic | Case Reports |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331257/ https://www.ncbi.nlm.nih.gov/pubmed/28265379 http://dx.doi.org/10.1002/ccr3.832 |
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