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A neuron autonomous role for the familial dysautonomia gene ELP1 in sympathetic and sensory target tissue innervation

Familial dysautonomia (FD) is characterized by severe and progressive sympathetic and sensory neuron loss caused by a highly conserved germline point mutation of the human ELP1/IKBKAP gene. Elp1 is a subunit of the hetero-hexameric transcriptional elongator complex, but how it functions in disease-v...

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Detalles Bibliográficos
Main Authors: Jackson, Marisa Z., Gruner, Katherine A., Qin, Charles, Tourtellotte, Warren G.
Formato: Artigo
Idioma:Inglês
Publicado: The Company of Biologists 2014
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4050699/
https://ncbi.nlm.nih.gov/pubmed/24917501
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dev.107797
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