Functional analysis of mutations in TGIF associated with holoprosencephaly

Holoprosencephaly (HPE) is the most common structural malformation of the forebrain and face in humans. Our current understanding of the pathogenesis of HPE attempts to integrate genetic susceptibility, evidenced by mutations in the known HPE genes, with the epigenetic influence of environmental fac...

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Detalhes bibliográficos
Main Authors: El-Jaick, Kenia B., Powers, Shannon E., Bartholin, Laurent, Myers, Kenneth R., Hahn, Jin, Orioli, Ieda M., Ouspenskaia, Maia, Lacbawan, Felicitas, Roessler, Erich, Wotton, David, Muenke, Maximilian
Formato: Artigo
Idioma:Inglês
Publicado em: 2006
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1820763/
https://ncbi.nlm.nih.gov/pubmed/16962354
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2006.07.011
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