Document Detail


Defective N-linked protein glycosylation pathway in congenital myasthenic syndromes.
MedLine Citation:
PMID:  23436500     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Authors:
Henry Houlden
Publication Detail:
Type:  Comment; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Brain : a journal of neurology     Volume:  136     ISSN:  1460-2156     ISO Abbreviation:  Brain     Publication Date:  2013 Mar 
Date Detail:
Created Date:  2013-02-25     Completed Date:  2013-04-23     Revised Date:  2014-03-06    
Medline Journal Info:
Nlm Unique ID:  0372537     Medline TA:  Brain     Country:  England    
Other Details:
Languages:  eng     Pagination:  692-5     Citation Subset:  AIM; IM    
Export Citation:
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MeSH Terms
Descriptor/Qualifier:
Female
Humans
Male
Myasthenic Syndromes, Congenital / genetics*,  physiopathology*
N-Acetylglucosaminyltransferases / genetics*
Grant Support
ID/Acronym/Agency:
G0802760//Medical Research Council; //Medical Research Council
Chemical
Reg. No./Substance:
EC 2.4.1.-/N-Acetylglucosaminyltransferases
Comments/Corrections
Comment On:
Brain. 2013 Mar;136(Pt 3):944-56   [PMID:  23404334 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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