Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment (Journal of Human Genetics, (2020), 65, 2, (187-192), 10.1038/s10038-019-0691-4)

Khurram Liaqat; Shabir Hussain; Muhammad Bilal; Abdul Nasir; Anushree Acharya; Raja Hussain Ali; Shoaib Nawaz; Muhammad Umair; Isabelle Schrauwen; Wasim Ahmad; Suzanne M. Leal

doi:10.1038/s10038-021-00951-9

Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment (Journal of Human Genetics, (2020), 65, 2, (187-192), 10.1038/s10038-019-0691-4)

Khurram Liaqat
, Shabir Hussain
, Muhammad Bilal
, Abdul Nasir
, Anushree Acharya
, Raja Hussain Ali
, Shoaib Nawaz
, Muhammad Umair
, Isabelle Schrauwen
, Wasim Ahmad
, Suzanne M. Leal

Research output: Contribution to journal › Comment/debate › peer-review

Abstract

The article “Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment”, written by Khurram Liaqat, et al., was originally published electronically on the publisher’s internet portal on 28 October2019 without open access.

Original language	English (US)
Journal	Journal of human genetics
DOIs	https://doi.org/10.1038/s10038-021-00951-9
State	Accepted/In press - 2021
Externally published	Yes

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1038/s10038-021-00951-9

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Liaqat, K., Hussain, S., Bilal, M., Nasir, A., Acharya, A., Ali, R. H., Nawaz, S., Umair, M., Schrauwen, I., Ahmad, W., & Leal, S. M. (Accepted/In press). Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment (Journal of Human Genetics, (2020), 65, 2, (187-192), 10.1038/s10038-019-0691-4). Journal of human genetics. https://doi.org/10.1038/s10038-021-00951-9

Liaqat, K, Hussain, S, Bilal, M, Nasir, A, Acharya, A, Ali, RH, Nawaz, S, Umair, M, Schrauwen, I, Ahmad, W & Leal, SM 2021, 'Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment (Journal of Human Genetics, (2020), 65, 2, (187-192), 10.1038/s10038-019-0691-4)', Journal of human genetics. https://doi.org/10.1038/s10038-021-00951-9

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title = "Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment (Journal of Human Genetics, (2020), 65, 2, (187-192), 10.1038/s10038-019-0691-4)",

abstract = "The article “Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment”, written by Khurram Liaqat, et al., was originally published electronically on the publisher{\textquoteright}s internet portal on 28 October2019 without open access.",

author = "Khurram Liaqat and Shabir Hussain and Muhammad Bilal and Abdul Nasir and Anushree Acharya and Ali, \{Raja Hussain\} and Shoaib Nawaz and Muhammad Umair and Isabelle Schrauwen and Wasim Ahmad and Leal, \{Suzanne M.\}",

note = "Publisher Copyright: {\textcopyright} The Author(s), under exclusive licence to The Japan Society of Human Genetics 2021",

year = "2021",

doi = "10.1038/s10038-021-00951-9",

language = "English (US)",

journal = "Journal of human genetics",

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T2 - Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment (Journal of Human Genetics, (2020), 65, 2, (187-192), 10.1038/s10038-019-0691-4)

AU - Liaqat, Khurram

AU - Hussain, Shabir

AU - Bilal, Muhammad

AU - Nasir, Abdul

AU - Acharya, Anushree

AU - Ali, Raja Hussain

AU - Nawaz, Shoaib

AU - Umair, Muhammad

AU - Schrauwen, Isabelle

AU - Ahmad, Wasim

AU - Leal, Suzanne M.

PY - 2021

Y1 - 2021

N2 - The article “Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment”, written by Khurram Liaqat, et al., was originally published electronically on the publisher’s internet portal on 28 October2019 without open access.

AB - The article “Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment”, written by Khurram Liaqat, et al., was originally published electronically on the publisher’s internet portal on 28 October2019 without open access.

UR - https://www.scopus.com/pages/publications/85115242589

UR - https://www.scopus.com/pages/publications/85115242589#tab=citedBy

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DO - 10.1038/s10038-021-00951-9

M3 - Comment/debate

C2 - 34526652

AN - SCOPUS:85115242589

SN - 1434-5161

JO - Journal of human genetics

JF - Journal of human genetics

ER -

Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment (Journal of Human Genetics, (2020), 65, 2, (187-192), 10.1038/s10038-019-0691-4)

Abstract

ASJC Scopus subject areas

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