Recommendations for Patient Screening in Ultra-Rare Inherited Metabolic Diseases: What Have We Learned From Niemann-Pick Disease Type C?
Orphanet Journal of Rare Diseases - United Kingdom
doi 10.1186/s13023-018-0985-1
Full Text
Open PDFAbstract
Available in full text
Date
January 21, 2019
Authors
Publisher
Springer Science and Business Media LLC