A Case of Fatal Type I Congenital Disorders of Glycosylation (CDG I) Associated With Low Dehydrodolichol Diphosphate Synthase (DHDDS) Activity
Orphanet Journal of Rare Diseases - United Kingdom
doi 10.1186/s13023-016-0468-1
Full Text
Open PDFAbstract
Available in full text
Date
June 24, 2016
Authors
Publisher
Springer Science and Business Media LLC