New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)

R Sallinen; A Vihola; L Bachinski; K Huoponen; H Haapasalo; P Hackman; S Zhang; M Sirito; H Kalimo; G Meola; N Horelli-Kuitunen; M Wessman; R Krahe; B. Udd

doi:10.1016/j.nmd.2004.01.002

New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)

R Sallinen
, A Vihola
, L Bachinski
, K Huoponen
, H Haapasalo
, P Hackman
, S Zhang
, M Sirito
, H Kalimo
, G Meola
, N Horelli-Kuitunen
, M Wessman
, R Krahe
, B. Udd

Department of Pathology

Research output: Contribution to journal › Article › Scientific › peer-review

45 Citations (Scopus)

Original language	English
Pages (from-to)	274-283
Journal	Neuromuscular Disorders
Volume	14
Issue number	4
DOIs	https://doi.org/10.1016/j.nmd.2004.01.002
Publication status	Published - 2004
Publication type	A1 Journal article-refereed

Access to Document

10.1016/j.nmd.2004.01.002

Cite this

Sallinen, R., Vihola, A., Bachinski, L., Huoponen, K., Haapasalo, H., Hackman, P., Zhang, S., Sirito, M., Kalimo, H., Meola, G., Horelli-Kuitunen, N., Wessman, M., Krahe, R., & Udd, B. (2004). New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2). Neuromuscular Disorders, 14(4), 274-283. https://doi.org/10.1016/j.nmd.2004.01.002

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author = "R Sallinen and A Vihola and L Bachinski and K Huoponen and H Haapasalo and P Hackman and S Zhang and M Sirito and H Kalimo and G Meola and N Horelli-Kuitunen and M Wessman and R Krahe and B. Udd",

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Sallinen, R, Vihola, A, Bachinski, L, Huoponen, K, Haapasalo, H, Hackman, P, Zhang, S, Sirito, M, Kalimo, H, Meola, G, Horelli-Kuitunen, N, Wessman, M, Krahe, R & Udd, B 2004, 'New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)', Neuromuscular Disorders, vol. 14, no. 4, pp. 274-283. https://doi.org/10.1016/j.nmd.2004.01.002

TY - JOUR

T1 - New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)

AU - Sallinen, R

AU - Vihola, A

AU - Bachinski, L

AU - Huoponen, K

AU - Haapasalo, H

AU - Hackman, P

AU - Zhang, S

AU - Sirito, M

AU - Kalimo, H

AU - Meola, G

AU - Horelli-Kuitunen, N

AU - Wessman, M

AU - Krahe, R

AU - Udd, B.

PY - 2004

Y1 - 2004

U2 - 10.1016/j.nmd.2004.01.002

DO - 10.1016/j.nmd.2004.01.002

M3 - Article

SN - 0960-8966

VL - 14

SP - 274

EP - 283

JO - Neuromuscular Disorders

JF - Neuromuscular Disorders

IS - 4

ER -