A novel mutation in a family with non-syndromic sensorineural hearing loss that disrupts the newly characterised OTOF long isoforms.

M. J. Houseman; A. P. Jackson; L. I. Al-Gazali; R. A. Badin; E. Roberts; R. F. Mueller

doi:10.1136/jmg.38.8.e25

A novel mutation in a family with non-syndromic sensorineural hearing loss that disrupts the newly characterised OTOF long isoforms.

M. J. Houseman, A. P. Jackson, L. I. Al-Gazali, R. A. Badin, E. Roberts, R. F. Mueller

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	E25
Journal	Journal of medical genetics
Volume	38
Issue number	8
DOIs	https://doi.org/10.1136/jmg.38.8.e25
Publication status	Published - Aug 2001
Externally published	Yes

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1136/jmg.38.8.e25

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title = "A novel mutation in a family with non-syndromic sensorineural hearing loss that disrupts the newly characterised OTOF long isoforms.",

author = "Houseman, {M. J.} and Jackson, {A. P.} and Al-Gazali, {L. I.} and Badin, {R. A.} and E. Roberts and Mueller, {R. F.}",

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AU - Al-Gazali, L. I.

AU - Badin, R. A.

AU - Roberts, E.

AU - Mueller, R. F.

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ER -

A novel mutation in a family with non-syndromic sensorineural hearing loss that disrupts the newly characterised OTOF long isoforms.

ASJC Scopus subject areas

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