A commentary on identification of the rare compound heterozygous variants in the NEB gene in a Korea...
A commentary on identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness
About this item
Full title
A commentary on identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness
Author / Creator
Publisher
England: Nature Publishing Group
Journal title
Journal of human genetics, 2015-03, Vol.60 (3), p.161-162
Language
English
Formats
Publication information
Publisher
England: Nature Publishing Group
Subjects
More information
Alternative Titles
Full title
A commentary on identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_1666990675
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1666990675
Other Identifiers
ISSN
1434-5161
E-ISSN
1435-232X
DOI
10.1038/jhg.2014.120
