Author:
Vacca Marcella,Filippini Francesco,Budillon Alberta,Rossi Valeria,Della Ragione Floriana,De Bonis Maria Luigia,Mercadante Grazia,Manzati Elisa,Gualandi Francesca,Bigoni Stefania,Trabanelli Cecilia,Pini Giorgio,Calzolari Elisa,Ferlini Alessandra,Meloni Ilaria,Hayek Giuseppe,Zappella Michele,Renieri Alessandra,D'Urso Michele,D'Esposito Maurizio,Macdonald Fiona,Kerr Alison,Dhanjal Seema,Hulten Maj
Subject
Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health
Reference21 articles.
1. On a unusual brain atrophy syndrome in hyperammonemia in childhood;Rett;Wien Med Wochenschr,1966
2. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases;Hagberg;Ann Neurol,1983
3. Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28;Sirianni;Am J Hum Genet,1998
4. Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2;D'Esposito;Mamm Genome,1996
5. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein2;Amir;Nat Genet,1999
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