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Autor:
Chris I. De Zeeuw, J. Hikke van Doorninck, Alar Karis, Frank Grosveld, J. Doug Engel, Martijn M. De Ruiter, Jacqueline van der Wees, Marjolein A.J. van Looij, Hans van der Burg, Helineth Elias, Bert G.A. van Zanten, Su San Liem, Dorota Kurek
Publikováno v:
Neurobiology of Disease, 16(1), 169-178. Academic Press
Neurobiology of Disease, Vol 16, Iss 1, Pp 169-178 (2004)
Neurobiology of Disease, Vol 16, Iss 1, Pp 169-178 (2004)
Patients with HDR syndrome suffer from hypoparathyroidism, deafness, and renal dysplasia due to a heterozygous deletion of the transcription factor GATA3. Since GATA3 is prominently expressed in both the inner ear and different parts of the auditory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69cdb7d14b1feb79385712466c7b3b1e
https://pure.eur.nl/en/publications/416f3bcf-f7c8-4543-97f0-b82168f0f049
https://pure.eur.nl/en/publications/416f3bcf-f7c8-4543-97f0-b82168f0f049