Standard
A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family. / Sanggaard, Kirsten Marie; Kjær, Klaus Wilbrandt; Eiberg, H.; Nurnberg, G.; Nurnberg, P.; Hoffman, K.; Jensen, H.; Sorum, C.; Rendtorff, Nanna Dahl; Tranebjaerg, L.
In:
American Journal of Medical Genetics. Part A, Vol. 146A, No. 8, 2008, p. 1017-1025.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Sanggaard, KM, Kjær, KW, Eiberg, H, Nurnberg, G, Nurnberg, P, Hoffman, K, Jensen, H, Sorum, C, Rendtorff, ND & Tranebjaerg, L 2008, 'A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family', American Journal of Medical Genetics. Part A, vol. 146A, no. 8, pp. 1017-1025.
APA
Sanggaard, K. M., Kjær, K. W., Eiberg, H., Nurnberg, G., Nurnberg, P., Hoffman, K., Jensen, H., Sorum, C., Rendtorff, N. D., & Tranebjaerg, L. (2008). A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family. American Journal of Medical Genetics. Part A, 146A(8), 1017-1025.
Vancouver
Sanggaard KM, Kjær KW, Eiberg H, Nurnberg G, Nurnberg P, Hoffman K et al. A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family. American Journal of Medical Genetics. Part A. 2008;146A(8):1017-1025.
Author
Sanggaard, Kirsten Marie ; Kjær, Klaus Wilbrandt ; Eiberg, H. ; Nurnberg, G. ; Nurnberg, P. ; Hoffman, K. ; Jensen, H. ; Sorum, C. ; Rendtorff, Nanna Dahl ; Tranebjaerg, L. / A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family. In: American Journal of Medical Genetics. Part A. 2008 ; Vol. 146A, No. 8. pp. 1017-1025.
Bibtex
@article{afc16fd0dcc911dd9473000ea68e967b,
title = "A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family",
abstract = "Udgivelsesdato: 2008/4/15",
author = "Sanggaard, {Kirsten Marie} and Kj{\ae}r, {Klaus Wilbrandt} and H. Eiberg and G. Nurnberg and P. Nurnberg and K. Hoffman and H. Jensen and C. Sorum and Rendtorff, {Nanna Dahl} and L. Tranebjaerg",
year = "2008",
language = "English",
volume = "146A",
pages = "1017--1025",
journal = "American Journal of Medical Genetics, Part A",
issn = "1552-4825",
publisher = "JohnWiley & Sons, Inc.",
number = "8",
}
RIS
TY - JOUR
T1 - A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family
AU - Sanggaard, Kirsten Marie
AU - Kjær, Klaus Wilbrandt
AU - Eiberg, H.
AU - Nurnberg, G.
AU - Nurnberg, P.
AU - Hoffman, K.
AU - Jensen, H.
AU - Sorum, C.
AU - Rendtorff, Nanna Dahl
AU - Tranebjaerg, L.
PY - 2008
Y1 - 2008
N2 - Udgivelsesdato: 2008/4/15
AB - Udgivelsesdato: 2008/4/15
M3 - Journal article
VL - 146A
SP - 1017
EP - 1025
JO - American Journal of Medical Genetics, Part A
JF - American Journal of Medical Genetics, Part A
SN - 1552-4825
IS - 8
ER -
