Analysis of Highly Conserved Regions of the 3'UTR of MECP2 Gene in Patients with Clinical Diagnosis of Rett Syndrome and Other Disorders Associated with Mental Retardation

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Detalhes bibliográficos
Autor principal: Santos, M (author)
Outros Autores: Yan, J (author), Temudo, T (author), Oliveira, G (author), Vieira, JP (author), Fen, J (author), Sommer, S (author), Maciel, P (author)
Formato: article
Idioma:eng
Publicado em: 2015
Assuntos:
3' Untranslated Regions/genetics
Intellectual Disability/genetics
Methyl-CpG-Binding Protein 2/genetics
Rett Syndrome/genetics
Genetic Variation
Genotype
Methyl-CpG-Binding
Methyl-CpG-Binding Protein 2/metabolism
Mutation
Phenotype
Polymerase Chain Reaction
Female
HDE NEU PED
Texto completo:http://hdl.handle.net/10400.17/2337
País:Brasil
Oai:oai:repositorio.chlc.min-saude.pt:10400.17/2337

Texto Completo

http://hdl.handle.net/10400.17/2337

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