Erratum: Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy (European Journal of Human Genetics (2012) 20 (897-904) DOI:10.1038/ejhg.2012.44)

Helen A.L. Tuppen; Karin Naess; Nancy G. Kennaway; Mazhor Al-Dosary; Nicole Lesko; John W. Yarham; Helene Bruhn; Rolf Wibom; Inger Nennesmo; Richard G. Weleber; Emma L. Blakely; Robert W. Taylor; Robert McFarland

doi:10.1038/ejhg.2012.123

Erratum: Mutations in the mitochondrial tRNA^Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy (European Journal of Human Genetics (2012) 20 (897-904) DOI:10.1038/ejhg.2012.44)

Helen A.L. Tuppen, Karin Naess, Nancy G. Kennaway, Mazhor Al-Dosary, Nicole Lesko, John W. Yarham, Helene Bruhn, Rolf Wibom, Inger Nennesmo, Richard G. Weleber, Emma L. Blakely, Robert W. Taylor, Robert McFarland

Research output: Contribution to journal › Comment/debate › peer-review

Original language	English (US)
Pages (from-to)	910
Number of pages	1
Journal	European Journal of Human Genetics
Volume	20
Issue number	8
DOIs	https://doi.org/10.1038/ejhg.2012.123
State	Published - Aug 2012
Externally published	Yes

ASJC Scopus subject areas

Genetics
Genetics(clinical)

Access to Document

10.1038/ejhg.2012.123

Cite this

Tuppen, H. A. L., Naess, K., Kennaway, N. G., Al-Dosary, M., Lesko, N., Yarham, J. W., Bruhn, H., Wibom, R., Nennesmo, I., Weleber, R. G., Blakely, E. L., Taylor, R. W., & McFarland, R. (2012). Erratum: Mutations in the mitochondrial tRNA^Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy (European Journal of Human Genetics (2012) 20 (897-904) DOI:10.1038/ejhg.2012.44). European Journal of Human Genetics, 20(8), 910. https://doi.org/10.1038/ejhg.2012.123

Erratum: Mutations in the mitochondrial tRNA^Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy (European Journal of Human Genetics (2012) 20 (897-904) DOI:10.1038/ejhg.2012.44). / Tuppen, Helen A.L.; Naess, Karin; Kennaway, Nancy G. et al.
In: European Journal of Human Genetics, Vol. 20, No. 8, 08.2012, p. 910.

Research output: Contribution to journal › Comment/debate › peer-review

Tuppen, HAL, Naess, K, Kennaway, NG, Al-Dosary, M, Lesko, N, Yarham, JW, Bruhn, H, Wibom, R, Nennesmo, I, Weleber, RG, Blakely, EL, Taylor, RW & McFarland, R 2012, 'Erratum: Mutations in the mitochondrial tRNA^Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy (European Journal of Human Genetics (2012) 20 (897-904) DOI:10.1038/ejhg.2012.44)', European Journal of Human Genetics, vol. 20, no. 8, pp. 910. https://doi.org/10.1038/ejhg.2012.123

Tuppen HAL, Naess K, Kennaway NG, Al-Dosary M, Lesko N, Yarham JW et al. Erratum: Mutations in the mitochondrial tRNA^Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy (European Journal of Human Genetics (2012) 20 (897-904) DOI:10.1038/ejhg.2012.44). European Journal of Human Genetics. 2012 Aug;20(8):910. doi: 10.1038/ejhg.2012.123

@article{b4a88ee185a947e88324aee6bf815bc7,

title = "Erratum: Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy (European Journal of Human Genetics (2012) 20 (897-904) DOI:10.1038/ejhg.2012.44)",

author = "Tuppen, {Helen A.L.} and Karin Naess and Kennaway, {Nancy G.} and Mazhor Al-Dosary and Nicole Lesko and Yarham, {John W.} and Helene Bruhn and Rolf Wibom and Inger Nennesmo and Weleber, {Richard G.} and Blakely, {Emma L.} and Taylor, {Robert W.} and Robert McFarland",

year = "2012",

month = aug,

doi = "10.1038/ejhg.2012.123",

language = "English (US)",

volume = "20",

pages = "910",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

number = "8",

}

TY - JOUR

T1 - Erratum

T2 - Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy (European Journal of Human Genetics (2012) 20 (897-904) DOI:10.1038/ejhg.2012.44)

AU - Tuppen, Helen A.L.

AU - Naess, Karin

AU - Kennaway, Nancy G.

AU - Al-Dosary, Mazhor

AU - Lesko, Nicole

AU - Yarham, John W.

AU - Bruhn, Helene

AU - Wibom, Rolf

AU - Nennesmo, Inger

AU - Weleber, Richard G.

AU - Blakely, Emma L.

AU - Taylor, Robert W.

AU - McFarland, Robert

PY - 2012/8

Y1 - 2012/8

UR - http://www.scopus.com/inward/record.url?scp=84864133901&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84864133901&partnerID=8YFLogxK

U2 - 10.1038/ejhg.2012.123

DO - 10.1038/ejhg.2012.123

M3 - Comment/debate

AN - SCOPUS:84864133901

SN - 1018-4813

VL - 20

SP - 910

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 8

ER -

Erratum: Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy (European Journal of Human Genetics (2012) 20 (897-904) DOI:10.1038/ejhg.2012.44)

ASJC Scopus subject areas

Access to Document

Other files and links

Cite this

Erratum: Mutations in the mitochondrial tRNA^Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy (European Journal of Human Genetics (2012) 20 (897-904) DOI:10.1038/ejhg.2012.44)