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Mutation spectrum of CYP21A2 and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850078/ http://dx.doi.org/10.1186/1687-9856-2013-S1-P128 |
| _version_ | 1782294033014456320 |
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| author | Dung, Vu Chi Khanh, Tran Van Fukami, Maki Phuong, Le Thi Ha, Nguyen Thi Liem, Nguyen Thanh Van, Ta Thanh |
| author_facet | Dung, Vu Chi Khanh, Tran Van Fukami, Maki Phuong, Le Thi Ha, Nguyen Thi Liem, Nguyen Thanh Van, Ta Thanh |
| author_sort | Dung, Vu Chi |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-3850078 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2013 |
| publisher | BioMed Central |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-38500782013-12-17 Mutation spectrum of CYP21A2 and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency Dung, Vu Chi Khanh, Tran Van Fukami, Maki Phuong, Le Thi Ha, Nguyen Thi Liem, Nguyen Thanh Van, Ta Thanh Int J Pediatr Endocrinol Poster Presentation BioMed Central 2013 2013-10-03 /pmc/articles/PMC3850078/ http://dx.doi.org/10.1186/1687-9856-2013-S1-P128 Text en Copyright © 2013 Dung et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
| spellingShingle | Poster Presentation Dung, Vu Chi Khanh, Tran Van Fukami, Maki Phuong, Le Thi Ha, Nguyen Thi Liem, Nguyen Thanh Van, Ta Thanh Mutation spectrum of CYP21A2 and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency |
| title | Mutation spectrum of CYP21A2 and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency |
| title_full | Mutation spectrum of CYP21A2 and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency |
| title_fullStr | Mutation spectrum of CYP21A2 and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency |
| title_full_unstemmed | Mutation spectrum of CYP21A2 and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency |
| title_short | Mutation spectrum of CYP21A2 and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency |
| title_sort | mutation spectrum of cyp21a2 and correlation between genotype – phenotype in 81 vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency |
| topic | Poster Presentation |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850078/ http://dx.doi.org/10.1186/1687-9856-2013-S1-P128 |
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