Cargando…
A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455050/ https://www.ncbi.nlm.nih.gov/pubmed/28524840 http://dx.doi.org/10.4103/0366-6999.206348 |
_version_ | 1783240970972692480 |
---|---|
author | Chu, Xue-Ying Li, Yue-Peng Nie, Min Wang, Ou Jiang, Yan Li, Mei Xia, Wei-Bo Xing, Xiao-Ping |
author_facet | Chu, Xue-Ying Li, Yue-Peng Nie, Min Wang, Ou Jiang, Yan Li, Mei Xia, Wei-Bo Xing, Xiao-Ping |
author_sort | Chu, Xue-Ying |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-5455050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54550502017-06-06 A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome Chu, Xue-Ying Li, Yue-Peng Nie, Min Wang, Ou Jiang, Yan Li, Mei Xia, Wei-Bo Xing, Xiao-Ping Chin Med J (Engl) Clinical Practice Medknow Publications & Media Pvt Ltd 2017-06-05 /pmc/articles/PMC5455050/ /pubmed/28524840 http://dx.doi.org/10.4103/0366-6999.206348 Text en Copyright: © 2017 Chinese Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Clinical Practice Chu, Xue-Ying Li, Yue-Peng Nie, Min Wang, Ou Jiang, Yan Li, Mei Xia, Wei-Bo Xing, Xiao-Ping A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome |
title | A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome |
title_full | A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome |
title_fullStr | A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome |
title_full_unstemmed | A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome |
title_short | A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome |
title_sort | novel de novo gata-binding protein 3 mutation in a patient with hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome |
topic | Clinical Practice |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455050/ https://www.ncbi.nlm.nih.gov/pubmed/28524840 http://dx.doi.org/10.4103/0366-6999.206348 |
work_keys_str_mv | AT chuxueying anoveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT liyuepeng anoveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT niemin anoveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT wangou anoveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT jiangyan anoveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT limei anoveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT xiaweibo anoveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT xingxiaoping anoveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT chuxueying noveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT liyuepeng noveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT niemin noveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT wangou noveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT jiangyan noveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT limei noveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT xiaweibo noveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome AT xingxiaoping noveldenovogatabindingprotein3mutationinapatientwithhypoparathyroidismsensorineuraldeafnessandrenaldysplasiasyndrome |