MUTATION DETECTION CORE
- 3 Anni 2000/2003
- 76.639€ Totale Fondi
Descrizione non disponibile
Pubblicazioni Scientifiche
- EUROPEAN JOURNAL OF HUMAN GENETICS
Clinical variability in calpainopathy: What makes the difference?
- HUMAN GENETICS
Analysis of 22 deletion breakpoints in dystrophin intron 49
- INTERNATIONAL JOURNAL OF OBESITY
Low frequency of melanocortin-4 receptor (MC4R) mutations in a Mediterranean population with early-onset obesity
