Publication
Title
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy
Author
Abstract
Language
English
Source (journal)
The American journal of human genetics / American Society of Human Genetics [Bethesda, Md] - New York, N.Y., 1949, currens
Publication
New York, N.Y. : 2013
ISSN
0002-9297 [print]
1537-6605 [online]
Volume/pages
93:1(2013), p. 6-18
ISI
000321804500001
Full text (Publisher's DOI)
UAntwerpen
Faculty/Department
Research group
Publication type
Subject
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identification
Creation 10.09.2013
Last edited 18.10.2018
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