Standard
Genetic correction of merosin deficiency in the dy2J mouse model of congenital muscular dystrophy. Partial genetic correction in two models. / Kuang, W.; Xu, H.; Vachon, P.H.; Liu, L.; Loechel, F.; Wewer, Ulla M.; Engvall, E.
I:
Journal of Clinical Investigation, Nr. 102, 1998, s. 844-852.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
Kuang, W, Xu, H, Vachon, PH, Liu, L, Loechel, F, Wewer, UM & Engvall, E 1998, 'Genetic correction of merosin deficiency in the dy2J mouse model of congenital muscular dystrophy. Partial genetic correction in two models', Journal of Clinical Investigation, nr. 102, s. 844-852.
APA
Kuang, W., Xu, H., Vachon, P. H., Liu, L., Loechel, F., Wewer, U. M., & Engvall, E. (1998). Genetic correction of merosin deficiency in the dy2J mouse model of congenital muscular dystrophy. Partial genetic correction in two models. Journal of Clinical Investigation, (102), 844-852.
Vancouver
Kuang W, Xu H, Vachon PH, Liu L, Loechel F, Wewer UM o.a. Genetic correction of merosin deficiency in the dy2J mouse model of congenital muscular dystrophy. Partial genetic correction in two models. Journal of Clinical Investigation. 1998;(102):844-852.
Author
Kuang, W. ; Xu, H. ; Vachon, P.H. ; Liu, L. ; Loechel, F. ; Wewer, Ulla M. ; Engvall, E. / Genetic correction of merosin deficiency in the dy2J mouse model of congenital muscular dystrophy. Partial genetic correction in two models. I: Journal of Clinical Investigation. 1998 ; Nr. 102. s. 844-852.
Bibtex
@article{a1ddd58074c911dbbee902004c4f4f50,
title = "Genetic correction of merosin deficiency in the dy2J mouse model of congenital muscular dystrophy. Partial genetic correction in two models",
author = "W. Kuang and H. Xu and P.H. Vachon and L. Liu and F. Loechel and Wewer, {Ulla M.} and E. Engvall",
year = "1998",
language = "English",
pages = "844--852",
journal = "Journal of Clinical Investigation",
issn = "0021-9738",
publisher = "American Society for Clinical Investigation",
number = "102",
}
RIS
TY - JOUR
T1 - Genetic correction of merosin deficiency in the dy2J mouse model of congenital muscular dystrophy. Partial genetic correction in two models
AU - Kuang, W.
AU - Xu, H.
AU - Vachon, P.H.
AU - Liu, L.
AU - Loechel, F.
AU - Wewer, Ulla M.
AU - Engvall, E.
PY - 1998
Y1 - 1998
M3 - Journal article
SP - 844
EP - 852
JO - Journal of Clinical Investigation
JF - Journal of Clinical Investigation
SN - 0021-9738
IS - 102
ER -
