Newborn screening in Fabry disease: what can be achieved with early diagnosis?
Clin Ther
.
2008:30 Suppl B:S41.
doi: 10.1016/s0149-2918(08)80035-5.
Author
Olaf A Bodamer
1
Affiliation
1
Division of Biochemical Genetics, University Children's Hospital, Währinger Gürtel 18-20, Vienna, Austria. olaf.bodamer@meduniwien.ac.at
PMID:
18395134
DOI:
10.1016/s0149-2918(08)80035-5
No abstract available
MeSH terms
Biomarkers
Fabry Disease / diagnosis*
Fabry Disease / therapy
Humans
Infant, Newborn
Lysosomal Storage Diseases / diagnosis
Neonatal Screening*
Tandem Mass Spectrometry
Substances
Biomarkers