| Literature DB >> 8596684 |
S J Schwarzenberg1, H L Sharp.
Abstract
Wilson's disease, genetic and neonatal hemochromatosis, protoporphyria, tyrosinemia, and alpha1-antitrypsin deficiency are updated. Cost effectiveness of screening is discussed. Current therapies are evaluated, including the role of transplantation. The molecular biologic technique PCR is covered. Gene therapy is introduced.Entities:
Mesh：
Year: 1996 PMID： 8596684 DOI： 10.1016/s0031-3955(05)70396-5
Source DB: PubMed Journal: Pediatr Clin North Am ISSN： 0031-3955 Impact factor: 3.278