HARS2 sequence variants identified in young individuals with severe sensorineural hearing impairment

H. Karstensen; N. Rendtorff; L. Hindhede; A. Stein; R. Hartmann-Petersen; K. Lindorff-Larsen; A. Hojland; M. Petersen; L. Tranebjaerg

HARS2 sequence variants identified in young individuals with severe sensorineural hearing impairment

H. Karstensen, N. Rendtorff, L. Hindhede, A. Stein, R. Hartmann-Petersen, K. Lindorff-Larsen, A. Hojland, M. Petersen, L. Tranebjaerg

Publikation: Bidrag til tidsskrift › Konferenceabstrakt i tidsskrift › Forskning › peer review

Originalsprog	Engelsk
Artikelnummer	P02.18A
Tidsskrift	European Journal of Human Genetics
Vol/bind	27
Udgave nummer	Suppl. 1
Sider (fra-til)	50-51
Antal sider	2
ISSN	1018-4813
Status	Udgivet - jul. 2019
Begivenhed	51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) - Milano, Italien Varighed: 16 jun. 2018 → 19 jun. 2018 Konferencens nummer: 51 https://2018.eshg.org/

Konference

Konference	51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)
Nummer	51
Land/Område	Italien
By	Milano
Periode	16/06/2018 → 19/06/2018
Internetadresse	https://2018.eshg.org/

Adgang til dokumentet

https://www.nature.com/articles/s41431-019-0404-7

AUB Link

Søg efter materialet i Aalborg Universitetsbiblioteks søgemaskine

Citationsformater

Karstensen, H., Rendtorff, N., Hindhede, L., Stein, A., Hartmann-Petersen, R., Lindorff-Larsen, K., Hojland, A., Petersen, M., & Tranebjaerg, L. (2019). HARS2 sequence variants identified in young individuals with severe sensorineural hearing impairment. European Journal of Human Genetics, 27(Suppl. 1), 50-51. Artikel P02.18A. https://www.nature.com/articles/s41431-019-0404-7

@article{73fe28ce981846dcbb2d2b493d9e165d,

title = "HARS2 sequence variants identified in young individuals with severe sensorineural hearing impairment",

author = "H. Karstensen and N. Rendtorff and L. Hindhede and A. Stein and R. Hartmann-Petersen and K. Lindorff-Larsen and A. Hojland and M. Petersen and L. Tranebjaerg",

year = "2019",

month = jul,

language = "English",

volume = "27",

pages = "50--51",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

number = "Suppl. 1",

note = "51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) ; Conference date: 16-06-2018 Through 19-06-2018",

url = "https://2018.eshg.org/",

}

Karstensen, H, Rendtorff, N, Hindhede, L, Stein, A, Hartmann-Petersen, R, Lindorff-Larsen, K, Hojland, A, Petersen, M & Tranebjaerg, L 2019, 'HARS2 sequence variants identified in young individuals with severe sensorineural hearing impairment', European Journal of Human Genetics, bind 27, nr. Suppl. 1, P02.18A, s. 50-51. <https://www.nature.com/articles/s41431-019-0404-7>

TY - ABST

T1 - HARS2 sequence variants identified in young individuals with severe sensorineural hearing impairment

AU - Karstensen, H.

AU - Rendtorff, N.

AU - Hindhede, L.

AU - Stein, A.

AU - Hartmann-Petersen, R.

AU - Lindorff-Larsen, K.

AU - Hojland, A.

AU - Petersen, M.

AU - Tranebjaerg, L.

N1 - Conference code: 51

PY - 2019/7

Y1 - 2019/7

M3 - Conference abstract in journal

SN - 1018-4813

VL - 27

SP - 50

EP - 51

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - Suppl. 1

M1 - P02.18A

T2 - 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)

Y2 - 16 June 2018 through 19 June 2018

ER -