Cargando…
Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment
| Autores principales: | , , , , , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer Singapore
2021
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9119233/ https://www.ncbi.nlm.nih.gov/pubmed/34526652 http://dx.doi.org/10.1038/s10038-021-00951-9 |
| _version_ | 1784710661705564160 |
|---|---|
| author | Liaqat, Khurram Hussain, Shabir Bilal, Muhammad Nasir, Abdul Acharya, Anushree Ali, Raja Hussain Nawaz, Shoaib Umair, Muhammad Schrauwen, Isabelle Ahmad, Wasim Leal, Suzanne M. |
| author_facet | Liaqat, Khurram Hussain, Shabir Bilal, Muhammad Nasir, Abdul Acharya, Anushree Ali, Raja Hussain Nawaz, Shoaib Umair, Muhammad Schrauwen, Isabelle Ahmad, Wasim Leal, Suzanne M. |
| author_sort | Liaqat, Khurram |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-9119233 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2021 |
| publisher | Springer Singapore |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-91192332022-05-20 Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment Liaqat, Khurram Hussain, Shabir Bilal, Muhammad Nasir, Abdul Acharya, Anushree Ali, Raja Hussain Nawaz, Shoaib Umair, Muhammad Schrauwen, Isabelle Ahmad, Wasim Leal, Suzanne M. J Hum Genet Correction Springer Singapore 2021-09-16 2022 /pmc/articles/PMC9119233/ /pubmed/34526652 http://dx.doi.org/10.1038/s10038-021-00951-9 Text en © The Author(s), under exclusive licence to The Japan Society of Human Genetics 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
| spellingShingle | Correction Liaqat, Khurram Hussain, Shabir Bilal, Muhammad Nasir, Abdul Acharya, Anushree Ali, Raja Hussain Nawaz, Shoaib Umair, Muhammad Schrauwen, Isabelle Ahmad, Wasim Leal, Suzanne M. Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment |
| title | Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment |
| title_full | Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment |
| title_fullStr | Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment |
| title_full_unstemmed | Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment |
| title_short | Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment |
| title_sort | correction: further evidence of involvement of tmem132e in autosomal recessive nonsyndromic hearing impairment |
| topic | Correction |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9119233/ https://www.ncbi.nlm.nih.gov/pubmed/34526652 http://dx.doi.org/10.1038/s10038-021-00951-9 |
| work_keys_str_mv | AT liaqatkhurram correctionfurtherevidenceofinvolvementoftmem132einautosomalrecessivenonsyndromichearingimpairment AT hussainshabir correctionfurtherevidenceofinvolvementoftmem132einautosomalrecessivenonsyndromichearingimpairment AT bilalmuhammad correctionfurtherevidenceofinvolvementoftmem132einautosomalrecessivenonsyndromichearingimpairment AT nasirabdul correctionfurtherevidenceofinvolvementoftmem132einautosomalrecessivenonsyndromichearingimpairment AT acharyaanushree correctionfurtherevidenceofinvolvementoftmem132einautosomalrecessivenonsyndromichearingimpairment AT alirajahussain correctionfurtherevidenceofinvolvementoftmem132einautosomalrecessivenonsyndromichearingimpairment AT nawazshoaib correctionfurtherevidenceofinvolvementoftmem132einautosomalrecessivenonsyndromichearingimpairment AT umairmuhammad correctionfurtherevidenceofinvolvementoftmem132einautosomalrecessivenonsyndromichearingimpairment AT schrauwenisabelle correctionfurtherevidenceofinvolvementoftmem132einautosomalrecessivenonsyndromichearingimpairment AT ahmadwasim correctionfurtherevidenceofinvolvementoftmem132einautosomalrecessivenonsyndromichearingimpairment AT lealsuzannem correctionfurtherevidenceofinvolvementoftmem132einautosomalrecessivenonsyndromichearingimpairment |