Novel OTOA mutations cause autosomal recessive non‐syndromic hearing impairment in Pakistani families. (23rd November 2012)

Record Type:: Journal Article
Title:: Novel OTOA mutations cause autosomal recessive non‐syndromic hearing impairment in Pakistani families. (23rd November 2012)
Main Title:: Novel OTOA mutations cause autosomal recessive non‐syndromic hearing impairment in Pakistani families
Authors:: Lee, K
Chiu, I
Santos‐Cortez, RLP
Basit, S
Khan, S
Azeem, Z
Andrade, PB
Kim, SS
Ahmad, W
Leal, SM
Abstract:
Is Part Of:: Clinical genetics. Volume 84:Number 3(2013:Sep.)
Journal:: Clinical genetics
Issue:: Volume 84:Number 3(2013:Sep.)
Issue Display:: Volume 84, Issue 3 (2013)
Year:: 2013
Volume:: 84
Issue:: 3
Issue Sort Value:: 2013-0084-0003-0000
Page Start:: 294
Page End:: 296
Publication Date:: 2012-11-23
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.12047 ↗
Languages:: English
ISSNs:: 0009-9163
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3286.287000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 38.xml