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A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect. / Thiselton, D.L.; Alexander, C.; Morris, A.; Brooks, S.; Rosenberg, T.; Eiberg, Hans Rudolf Lytchoff; Kjer, B.; Bhattacharya, S.S.; Votruba, M.
In:
Hum. Genet., No. vol. 109, 2001, p. 498-502.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Thiselton, DL, Alexander, C, Morris, A, Brooks, S, Rosenberg, T, Eiberg, HRL, Kjer, B, Bhattacharya, SS & Votruba, M 2001, 'A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect', Hum. Genet., no. vol. 109, pp. 498-502.
APA
Thiselton, D. L., Alexander, C., Morris, A., Brooks, S., Rosenberg, T., Eiberg, H. R. L., Kjer, B., Bhattacharya, S. S., & Votruba, M. (2001). A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect. Hum. Genet., (vol. 109), 498-502.
Vancouver
Thiselton DL, Alexander C, Morris A, Brooks S, Rosenberg T, Eiberg HRL et al. A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect. Hum. Genet. 2001;(vol. 109):498-502.
Author
Thiselton, D.L. ; Alexander, C. ; Morris, A. ; Brooks, S. ; Rosenberg, T. ; Eiberg, Hans Rudolf Lytchoff ; Kjer, B. ; Bhattacharya, S.S. ; Votruba, M. / A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect. In: Hum. Genet. 2001 ; No. vol. 109. pp. 498-502.
Bibtex
@article{f04e8a6074c511dbbee902004c4f4f50,
title = "A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect",
author = "D.L. Thiselton and C. Alexander and A. Morris and S. Brooks and T. Rosenberg and Eiberg, {Hans Rudolf Lytchoff} and B. Kjer and S.S. Bhattacharya and M. Votruba",
year = "2001",
language = "English",
pages = "498--502",
journal = "Hum. Genet.",
publisher = "Springer",
number = "vol. 109",
}
RIS
TY - JOUR
T1 - A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect
AU - Thiselton, D.L.
AU - Alexander, C.
AU - Morris, A.
AU - Brooks, S.
AU - Rosenberg, T.
AU - Eiberg, Hans Rudolf Lytchoff
AU - Kjer, B.
AU - Bhattacharya, S.S.
AU - Votruba, M.
PY - 2001
Y1 - 2001
M3 - Journal article
SP - 498
EP - 502
JO - Hum. Genet.
JF - Hum. Genet.
IS - vol. 109
ER -
