Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.

Patients with disorders involving imprinted genes such as Angelman syndrome (AS) and Prader-Willi syndrome (PWS) can have a mutation in the imprinting mechanism. Previously, we identified an imprinting center (IC) within chromosome 15q11-ql3 and proposed that IC mutations block resetting of the impr...

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Detalhes bibliográficos
Main Authors: Saitoh, S, Buiting, K, Rogan, P K, Buxton, J L, Driscoll, D J, Arnemann, J, König, R, Malcolm, S, Horsthemke, B, Nicholls, R D
Formato: Artigo
Idioma:Inglês
Publicado em: 1996
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC38830/
https://ncbi.nlm.nih.gov/pubmed/8755558
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