Genetic Hearing Loss
Editat de Patrick J. Willemsen Limba Engleză Paperback – 17 oct 2019
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Specificații
ISBN-13: 9780367394929
ISBN-10: 0367394928
Pagini: 504
Dimensiuni: 152 x 229 mm
Greutate: 0.93 kg
Ediția:1
Editura: CRC Press
Colecția CRC Press
ISBN-10: 0367394928
Pagini: 504
Dimensiuni: 152 x 229 mm
Greutate: 0.93 kg
Ediția:1
Editura: CRC Press
Colecția CRC Press
Public țintă
Professional Practice & Development and Professional ReferenceCuprins
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.
Descriere
Genetic Hearing Loss branches into syndromic and nonsyndromic categorical directions in its coverage of the genetics behind hearing loss.