Standard
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene. / Eiberg, Hans Rudolf Lytchoff; Hansen, Lars; Kjer, B.; Hansen, T.; Pedersen, O.; Bille, M.; Rosenberg, T.; Tranebjaerg, L.
In:
Journal of Medical Genetics, Vol. 43, No. 5, 2006, p. 435-440.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Eiberg, HRL, Hansen, L, Kjer, B, Hansen, T, Pedersen, O, Bille, M, Rosenberg, T & Tranebjaerg, L 2006, 'Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene', Journal of Medical Genetics, vol. 43, no. 5, pp. 435-440.
APA
Eiberg, H. R. L., Hansen, L., Kjer, B., Hansen, T., Pedersen, O., Bille, M., Rosenberg, T., & Tranebjaerg, L. (2006). Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene. Journal of Medical Genetics, 43(5), 435-440.
Vancouver
Eiberg HRL, Hansen L, Kjer B, Hansen T, Pedersen O, Bille M et al. Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene. Journal of Medical Genetics. 2006;43(5):435-440.
Author
Eiberg, Hans Rudolf Lytchoff ; Hansen, Lars ; Kjer, B. ; Hansen, T. ; Pedersen, O. ; Bille, M. ; Rosenberg, T. ; Tranebjaerg, L. / Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene. In: Journal of Medical Genetics. 2006 ; Vol. 43, No. 5. pp. 435-440.
Bibtex
@article{d7cb90a070eb11dcbee902004c4f4f50,
title = "Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene",
abstract = "Udgivelsesdato: 2006/5",
author = "Eiberg, {Hans Rudolf Lytchoff} and Lars Hansen and B. Kjer and T. Hansen and O. Pedersen and M. Bille and T. Rosenberg and L. Tranebjaerg",
year = "2006",
language = "English",
volume = "43",
pages = "435--440",
journal = "Journal of Medical Genetics",
issn = "0022-2593",
publisher = "B M J Group",
number = "5",
}
RIS
TY - JOUR
T1 - Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene
AU - Eiberg, Hans Rudolf Lytchoff
AU - Hansen, Lars
AU - Kjer, B.
AU - Hansen, T.
AU - Pedersen, O.
AU - Bille, M.
AU - Rosenberg, T.
AU - Tranebjaerg, L.
PY - 2006
Y1 - 2006
N2 - Udgivelsesdato: 2006/5
AB - Udgivelsesdato: 2006/5
M3 - Journal article
VL - 43
SP - 435
EP - 440
JO - Journal of Medical Genetics
JF - Journal of Medical Genetics
SN - 0022-2593
IS - 5
ER -
