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A unique triadin exon deletion causing a null phenotype
| Autores principales: | , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6241331/ https://www.ncbi.nlm.nih.gov/pubmed/30479949 http://dx.doi.org/10.1016/j.hrcr.2018.07.014 |
| _version_ | 1783371759857172480 |
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| author | O’Callaghan, Barry M. Hancox, Jules C. Stuart, Alan G. Armstrong, Catherine Williams, Maggie M. Hills, Alison Pearce, Hazel Dent, Carolyn L. Gable, Mary Walsh, Mark A. |
| author_facet | O’Callaghan, Barry M. Hancox, Jules C. Stuart, Alan G. Armstrong, Catherine Williams, Maggie M. Hills, Alison Pearce, Hazel Dent, Carolyn L. Gable, Mary Walsh, Mark A. |
| author_sort | O’Callaghan, Barry M. |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-6241331 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2018 |
| publisher | Elsevier |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-62413312018-11-26 A unique triadin exon deletion causing a null phenotype O’Callaghan, Barry M. Hancox, Jules C. Stuart, Alan G. Armstrong, Catherine Williams, Maggie M. Hills, Alison Pearce, Hazel Dent, Carolyn L. Gable, Mary Walsh, Mark A. HeartRhythm Case Rep Case Report Elsevier 2018-08-04 /pmc/articles/PMC6241331/ /pubmed/30479949 http://dx.doi.org/10.1016/j.hrcr.2018.07.014 Text en Crown Copyright © 2018 Published by Elsevier Inc. on behalf of Heart Rhythm Society. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
| spellingShingle | Case Report O’Callaghan, Barry M. Hancox, Jules C. Stuart, Alan G. Armstrong, Catherine Williams, Maggie M. Hills, Alison Pearce, Hazel Dent, Carolyn L. Gable, Mary Walsh, Mark A. A unique triadin exon deletion causing a null phenotype |
| title | A unique triadin exon deletion causing a null phenotype |
| title_full | A unique triadin exon deletion causing a null phenotype |
| title_fullStr | A unique triadin exon deletion causing a null phenotype |
| title_full_unstemmed | A unique triadin exon deletion causing a null phenotype |
| title_short | A unique triadin exon deletion causing a null phenotype |
| title_sort | unique triadin exon deletion causing a null phenotype |
| topic | Case Report |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6241331/ https://www.ncbi.nlm.nih.gov/pubmed/30479949 http://dx.doi.org/10.1016/j.hrcr.2018.07.014 |
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