SECOND HUMAN PSEUDOAUTOSOMAL REGION: BIOLOGY, GENES AND IMPLICATIONS FOR THE PATHOGENESIS OF RETT SYNDROME
- 3 Anni 1999/2002
- 185.924€ Totale Fondi
Descrizione non disponibile
Pubblicazioni Scientifiche
- BRAIN & DEVELOPMENT
MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region
- GENOME RESEARCH
Complex events in the evolution of the human pseudoautosomal region 2 (PAR2)
- HUMAN MOLECULAR GENETICS
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region
- HUMAN MUTATION
DHPLC analysis of the MECP2 gene in Italian Rett patients
- JOURNAL OF MOLECULAR MEDICINE-JMM
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females