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Autor:
Heer, A.M. de, Collin, R.W.J., Huygen, P.L.M., Schraders, M., Oostrik, J., Rouwette, M., Kunst, H.P.M., Kremer, J.M.J., Cremers, C.W.R.J.
Publikováno v:
Audiology and Neuro-Otology, 16, 93-105
Audiology and Neuro-Otology, 16, 2, pp. 93-105
Audiology and Neuro-Otology, 16, 2, pp. 93-105
Item does not contain fulltext In a Dutch family with autosomal recessive hearing loss, genome-wide single-nucleotide polymorphism analysis mapped the genetic defect to the DFNB7/11 locus. A novel homozygous A-to-G change in the TMC1 gene was detecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5d0224f224c5d34a0cd4d8aff5ec5197
http://hdl.handle.net/2066/97261
http://hdl.handle.net/2066/97261
