Clinical and Genetic Studies of Hearing Impairment

Clinical and Genetic Studies of Hearing Impairment

Monogenic disorders offer a possibility for studies of genetic disturbances in hearing impairment—a knowledge which could be essential for development of future treatment options. In this thesis, the underlying genetic disturbances in neurofibromatosis 2 (NF2) and familial Meniere’s disease (FMD) we...

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Bibliographic Details
Main Author: Frykholm, Carina
Format: Doctoral Thesis
Language:English
Published: Uppsala universitet, Institutionen för kirurgiska vetenskaper 2007
Subjects:
Otorhinolaryngology
NF2
array-CGH
Meniere’s disease
PIK3C2G
X-linked
progressive
hearing impairment
Otorhinolaryngologi
Online Access:http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-8290
http://nbn-resolving.de/urn:isbn:978-91-554-7006-7

Internet

http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-8290
http://nbn-resolving.de/urn:isbn:978-91-554-7006-7

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