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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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Hlavní autoři: Jackson, Marisa Z., Gruner, Katherine A., Qin, Charles, Tourtellotte, Warren G.
Médium: Artigo
Jazyk:Inglês
Vydáno: The Company of Biologists 2014
Témata:
On-line přístup: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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