Publication
Title
Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores
Author
Language
English
Source (journal)
Human mutation. - New York, N.Y.
Publication
New York, N.Y. : 2008
ISSN
1059-7794
Volume/pages
29:5(2008), p. 670-678
ISI
000255385800012
Note
General: doi:10.1002/humu.20696
Full text (Publisher's DOI)
UAntwerpen
Faculty/Department
Research group
Publication type
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identification
Creation 08.10.2008
Last edited 10.09.2017
To cite this reference