A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment. / Lindquist, Susanne Granhøj; Hasholt, L.; Bahl, J.M.C.; Heegaard, N.H.H.; Andersen, B.B.; Nørremølle, Anne; Stokholm, J.; Schwartz, M.; Batbayli, M.; Laursen, Henning; Pardossi-Piquard, R.; Chen, F.; George-Hyslop, P. St; Waldemar, Gunhild; Nielsen, J.E.

I: European Journal of Neurology, Bind 15, Nr. 10, 2008, s. 1135-1139.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Lindquist, SG, Hasholt, L, Bahl, JMC, Heegaard, NHH, Andersen, BB, Nørremølle, A, Stokholm, J, Schwartz, M, Batbayli, M, Laursen, H, Pardossi-Piquard, R, Chen, F, George-Hyslop, PS, Waldemar, G & Nielsen, JE 2008, 'A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment', European Journal of Neurology, bind 15, nr. 10, s. 1135-1139.

APA

Lindquist, S. G., Hasholt, L., Bahl, J. M. C., Heegaard, N. H. H., Andersen, B. B., Nørremølle, A., Stokholm, J., Schwartz, M., Batbayli, M., Laursen, H., Pardossi-Piquard, R., Chen, F., George-Hyslop, P. S., Waldemar, G., & Nielsen, J. E. (2008). A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment. European Journal of Neurology, 15(10), 1135-1139.

Vancouver

Lindquist SG, Hasholt L, Bahl JMC, Heegaard NHH, Andersen BB, Nørremølle A o.a. A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment. European Journal of Neurology. 2008;15(10):1135-1139.

Author

Lindquist, Susanne Granhøj ; Hasholt, L. ; Bahl, J.M.C. ; Heegaard, N.H.H. ; Andersen, B.B. ; Nørremølle, Anne ; Stokholm, J. ; Schwartz, M. ; Batbayli, M. ; Laursen, Henning ; Pardossi-Piquard, R. ; Chen, F. ; George-Hyslop, P. St ; Waldemar, Gunhild ; Nielsen, J.E. / A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment. I: European Journal of Neurology. 2008 ; Bind 15, Nr. 10. s. 1135-1139.

Bibtex

@article{52b963e0dd7011ddb5fc000ea68e967b,
title = "A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment",
abstract = "Udgivelsesdato: 2008/10",
author = "Lindquist, {Susanne Granh{\o}j} and L. Hasholt and J.M.C. Bahl and N.H.H. Heegaard and B.B. Andersen and Anne N{\o}rrem{\o}lle and J. Stokholm and M. Schwartz and M. Batbayli and Henning Laursen and R. Pardossi-Piquard and F. Chen and George-Hyslop, {P. St} and Gunhild Waldemar and J.E. Nielsen",
year = "2008",
language = "English",
volume = "15",
pages = "1135--1139",
journal = "European Journal of Neurology",
issn = "1351-5101",
publisher = "Wiley-Blackwell",
number = "10",

}

RIS

TY - JOUR

T1 - A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment

AU - Lindquist, Susanne Granhøj

AU - Hasholt, L.

AU - Bahl, J.M.C.

AU - Heegaard, N.H.H.

AU - Andersen, B.B.

AU - Nørremølle, Anne

AU - Stokholm, J.

AU - Schwartz, M.

AU - Batbayli, M.

AU - Laursen, Henning

AU - Pardossi-Piquard, R.

AU - Chen, F.

AU - George-Hyslop, P. St

AU - Waldemar, Gunhild

AU - Nielsen, J.E.

PY - 2008

Y1 - 2008

N2 - Udgivelsesdato: 2008/10

AB - Udgivelsesdato: 2008/10

M3 - Journal article

VL - 15

SP - 1135

EP - 1139

JO - European Journal of Neurology

JF - European Journal of Neurology

SN - 1351-5101

IS - 10

ER -

ID: 9586759