MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients

Mutations in the coding sequence of the methyl-CpG-binding protein 2 gene (MECP2), which cause Rett syndrome (RTT), have been found in male and female autistic subjects without, however, a causal relation having unequivocally been established. In this study, the MECP2 gene was scanned in a Portugues...

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Detalhes bibliográficos
Autor principal: Coutinho, Ana M. (author)
Outros Autores: Oliveira, Guiomar (author), Katz, Cécile (author), Feng, Jinong (author), Yan, Jin (author), Yang, Chunmei (author), Marques, Carla (author), Ataíde, Assunção (author), Miguel, Teresa S. (author), Borges, Luís (author), Almeida, Joana (author), Correia, Catarina (author), Currais, António (author), Bento, Celeste (author), Mota-Vieira, Luísa (author), Temudo, Teresa (author), Santos, Mónica (author), Maciel, P. (author), Sommer, Steve S. (author), Vicente, Astrid M. (author)
Formato: article
Idioma:eng
Publicado em: 2007
Assuntos:
3' Untranslated Regions
Adolescent
Alanine
Autistic Disorder
Case-Control Studies
Child
Child, Preschool
DNA Mutational Analysis
Exons
Female
Gene Expression Regulation
Glycine
Humans
Introns
Male
Methyl-CpG-Binding Protein 2
Mutation, Missense
Open Reading Frames
Pedigree
RNA, Messenger
X Chromosome Inactivation
Autism
MECP2
3′UTR
exon 1
Detection of Virtually All Mutations‐SSCP
Ciências Médicas::Medicina Básica
Science & Technology
Texto completo:http://hdl.handle.net/1822/67669
País:Portugal
Oai:oai:repositorium.sdum.uminho.pt:1822/67669

Texto Completo

http://hdl.handle.net/1822/67669

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