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LPIN1 deficiency: A novel mutation associated with different phenotypes in the same family
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2016
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050266/ https://www.ncbi.nlm.nih.gov/pubmed/27722093 http://dx.doi.org/10.1016/j.ymgmr.2016.09.004 |
| _version_ | 1782457848182079488 |
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| author | Nunes, D Nogueira, C Lopes, A Chaves, P Rodrigues, E Cardoso, T Leão Teles, E Vilarinho, L |
| author_facet | Nunes, D Nogueira, C Lopes, A Chaves, P Rodrigues, E Cardoso, T Leão Teles, E Vilarinho, L |
| author_sort | Nunes, D |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-5050266 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2016 |
| publisher | Elsevier |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-50502662016-10-07 LPIN1 deficiency: A novel mutation associated with different phenotypes in the same family Nunes, D Nogueira, C Lopes, A Chaves, P Rodrigues, E Cardoso, T Leão Teles, E Vilarinho, L Mol Genet Metab Rep Letter to the Editor Elsevier 2016-10-02 /pmc/articles/PMC5050266/ /pubmed/27722093 http://dx.doi.org/10.1016/j.ymgmr.2016.09.004 Text en © 2016 The Authors 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 | Letter to the Editor Nunes, D Nogueira, C Lopes, A Chaves, P Rodrigues, E Cardoso, T Leão Teles, E Vilarinho, L LPIN1 deficiency: A novel mutation associated with different phenotypes in the same family |
| title | LPIN1 deficiency: A novel mutation associated with different phenotypes in the same family |
| title_full | LPIN1 deficiency: A novel mutation associated with different phenotypes in the same family |
| title_fullStr | LPIN1 deficiency: A novel mutation associated with different phenotypes in the same family |
| title_full_unstemmed | LPIN1 deficiency: A novel mutation associated with different phenotypes in the same family |
| title_short | LPIN1 deficiency: A novel mutation associated with different phenotypes in the same family |
| title_sort | lpin1 deficiency: a novel mutation associated with different phenotypes in the same family |
| topic | Letter to the Editor |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050266/ https://www.ncbi.nlm.nih.gov/pubmed/27722093 http://dx.doi.org/10.1016/j.ymgmr.2016.09.004 |
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