학술논문
A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment
Document Type
Article
Author
Del Castillo, F.J.; Rodríguez-Ballesteros, M.; Álvarez, A.; Aguirre, L.A.; Moreno-Pelayo, M.A.; Villamar, M.; Moreno, F.; Del Castillo, I.; Weil, D.; Petit, C.; Hutchin, T.; Leonardi, E.; Murgia, A.; De Oliveira, C.A.; Sartorato, E.L.; Azaiez, H.; Avenarius, M.R.; Smith, R.J.H.; Brownstein, Z.; Avraham, K.B.; Marlin, S.; Marlín, Y.; Pandya, A.; Nance, W.E.; Shahin, H.; Kanaan, M.; Siemering; Wuyts, W.; Van Camp, G.; Dahl, H.-H.M.
Source
In: Journal of Medical Genetics . (Journal of Medical Genetics, July 2005, 42(7):588-594)
Subject
Language
English
ISSN
00222593