Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

Z.M. Ahmed; S. Masmoudi; E. Kalay; I.A. Belyantseva; M.A. Mosrati; R.W. Collin; S. Riazuddin; M. Hmani-Aifa; H. Venselaar; M.N. Kawar; A. Tlili; A. van der Zwaag; S.Y. Khan; L. Ayadi; S.A. Riazuddin; R.J. Morrell; A.J. Griffith; I. Charfedine; R. Caylan; J. Oostrik; A. Karaguzel; A. Ghorbel; T.B. Friedman; H. Ayadi; H. Kremer

Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

Translated title of the contribution: Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

Z.M. Ahmed, S. Masmoudi, E. Kalay, I.A. Belyantseva, M.A. Mosrati, R.W. Collin, S. Riazuddin, M. Hmani-Aifa, H. Venselaar, M.N. Kawar, A. Tlili, A. van der Zwaag, S.Y. Khan, L. Ayadi, S.A. Riazuddin, R.J. Morrell, A.J. Griffith, I. Charfedine, R. Caylan, J. OostrikA. Karaguzel, A. Ghorbel, T.B. Friedman, H. Ayadi, H. Kremer

Translational Neuroscience

Research output: Contribution to journal › Article › Academic › peer-review

Translated title of the contribution	Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans
Original language	Undefined/Unknown
Pages (from-to)	1335-1340
Number of pages	6
Journal	Nature Genetics
Volume	40
Publication status	Published - 2008

Cite this

Ahmed, Z. M., Masmoudi, S., Kalay, E., Belyantseva, I. A., Mosrati, M. A., Collin, R. W., Riazuddin, S., Hmani-Aifa, M., Venselaar, H., Kawar, M. N., Tlili, A., van der Zwaag, A., Khan, S. Y., Ayadi, L., Riazuddin, S. A., Morrell, R. J., Griffith, A. J., Charfedine, I., Caylan, R., ... Kremer, H. (2008). Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. Nature Genetics, 40, 1335-1340.

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title = "Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans",

author = "Z.M. Ahmed and S. Masmoudi and E. Kalay and I.A. Belyantseva and M.A. Mosrati and R.W. Collin and S. Riazuddin and M. Hmani-Aifa and H. Venselaar and M.N. Kawar and A. Tlili and {van der Zwaag}, A. and S.Y. Khan and L. Ayadi and S.A. Riazuddin and R.J. Morrell and A.J. Griffith and I. Charfedine and R. Caylan and J. Oostrik and A. Karaguzel and A. Ghorbel and T.B. Friedman and H. Ayadi and H. Kremer",

year = "2008",

language = "Undefined/Unknown",

volume = "40",

pages = "1335--1340",

journal = "Nature Genetics",

issn = "1061-4036",

publisher = "Nature Publishing Group",

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Ahmed, ZM, Masmoudi, S, Kalay, E, Belyantseva, IA, Mosrati, MA, Collin, RW, Riazuddin, S, Hmani-Aifa, M, Venselaar, H, Kawar, MN, Tlili, A, van der Zwaag, A, Khan, SY, Ayadi, L, Riazuddin, SA, Morrell, RJ, Griffith, AJ, Charfedine, I, Caylan, R, Oostrik, J, Karaguzel, A, Ghorbel, A, Friedman, TB, Ayadi, H & Kremer, H 2008, 'Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans', Nature Genetics, vol. 40, pp. 1335-1340.

TY - JOUR

T1 - Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

AU - Ahmed, Z.M.

AU - Masmoudi, S.

AU - Kalay, E.

AU - Belyantseva, I.A.

AU - Mosrati, M.A.

AU - Collin, R.W.

AU - Riazuddin, S.

AU - Hmani-Aifa, M.

AU - Venselaar, H.

AU - Kawar, M.N.

AU - Tlili, A.

AU - van der Zwaag, A.

AU - Khan, S.Y.

AU - Ayadi, L.

AU - Riazuddin, S.A.

AU - Morrell, R.J.

AU - Griffith, A.J.

AU - Charfedine, I.

AU - Caylan, R.

AU - Oostrik, J.

AU - Karaguzel, A.

AU - Ghorbel, A.

AU - Friedman, T.B.

AU - Ayadi, H.

AU - Kremer, H.

PY - 2008

Y1 - 2008

M3 - Article

SN - 1061-4036

VL - 40

SP - 1335

EP - 1340

JO - Nature Genetics

JF - Nature Genetics

ER -