Genetic Hearing Loss

Herausgeber: Willems, Patrick J

• Broschiertes Buch

Produktbeschreibung

Genetic Hearing Loss branches into syndromic and nonsyndromic categorical directions in its coverage of the genetics behind hearing loss.

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Produktdetails

• Verlag: Taylor & Francis Ltd (Sales)
• Seitenzahl: 504
• Erscheinungstermin: 17. Oktober 2019
• Englisch
• Abmessung: 226mm x 152mm x 25mm
• Gewicht: 816g
• ISBN-13: 9780367394929
• ISBN-10: 0367394928
• Artikelnr.: 58054962

Autorenporträt

Patrick J. Willems

Inhaltsangabe

Hearing and hearing loss: normal development of the ear in the human and mouse
audiometric tests and diagnostic workup
classification and epidemiology of hearing loss
Syndromic hearing loss: Usher syndrome
pendred syndrome
Waardenburg syndrome
Nielsensyndrome
HDR syndrome
branchio-oto-renal syndrome
Treacher Collins syndrome
MYH9
mitochondrial hearingloss
Genes responsible for nonsyndromic hearing loss: gene localization and isolation in nonsyndromic hearing loss
connexins
myosin VI
K+ channel gene KCNQ4
COL11A2
POU-Domain transcription factors
a-Tectorin P. EYA4 DFNA 5 COCH Diaphanous
Claudin 14 CDH23 TMPRSS33
otosclerosis. Miscellaneous factors: mechanisms that regulate hair cell differentiation and regeneration
genetic testing - possibilitiesand attitudes.