Erratum: Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population (Journal of Human Genetics (2013) 58 (102-108) DIO: 10.1038/jhg.2012.143)

Zil E.Huma Bashir; Noreen Latief; Inna A. Belyantseva; Farheena Iqbal; Sheikh Amer Riazuddin; Shaheen N. Khan; Thomas B. Friedman; Saima Riazuddin

doi:10.1038/jhg.2013.85

Erratum: Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population (Journal of Human Genetics (2013) 58 (102-108) DIO: 10.1038/jhg.2012.143)

Zil E.Huma Bashir, Noreen Latief, Inna A. Belyantseva, Farheena Iqbal, Sheikh Amer Riazuddin, Shaheen N. Khan, Thomas B. Friedman, Saima Riazuddin

School of Medicine

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

Original language	English (US)
Pages (from-to)	641
Number of pages	1
Journal	Journal of Human Genetics
Volume	58
Issue number	9
DOIs	https://doi.org/10.1038/jhg.2013.85
State	Published - Sep 2013

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1038/jhg.2013.85

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Bashir, Z. E. H., Latief, N., Belyantseva, I. A., Iqbal, F., Amer Riazuddin, S., Khan, S. N., Friedman, T. B., & Riazuddin, S. (2013). Erratum: Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population (Journal of Human Genetics (2013) 58 (102-108) DIO: 10.1038/jhg.2012.143). Journal of Human Genetics, 58(9), 641. https://doi.org/10.1038/jhg.2013.85

Erratum: Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population (Journal of Human Genetics (2013) 58 (102-108) DIO: 10.1038/jhg.2012.143). / Bashir, Zil E.Huma; Latief, Noreen; Belyantseva, Inna A. et al.
In: Journal of Human Genetics, Vol. 58, No. 9, 09.2013, p. 641.

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

Bashir, ZEH, Latief, N, Belyantseva, IA, Iqbal, F, Amer Riazuddin, S, Khan, SN, Friedman, TB & Riazuddin, S 2013, 'Erratum: Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population (Journal of Human Genetics (2013) 58 (102-108) DIO: 10.1038/jhg.2012.143)', Journal of Human Genetics, vol. 58, no. 9, pp. 641. https://doi.org/10.1038/jhg.2013.85

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author = "Bashir, {Zil E.Huma} and Noreen Latief and Belyantseva, {Inna A.} and Farheena Iqbal and {Amer Riazuddin}, Sheikh and Khan, {Shaheen N.} and Friedman, {Thomas B.} and Saima Riazuddin",

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Erratum: Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population (Journal of Human Genetics (2013) 58 (102-108) DIO: 10.1038/jhg.2012.143)

ASJC Scopus subject areas

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