MicroRNA screening identifies a link between NOVA1 expression and a low level of IKAP in familial dysautonomia
Familial dysautonomia (FD) is a rare neurodegenerative disease caused by a mutation in intron 20 of the IKBKAP gene (c.2204+6T>C), leading to tissue-specific skipping of exon 20 and a decrease in the synthesis of the encoded protein IKAP (also known as ELP1). Small non-coding RNAs known as microRNAs...
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| Principais autores: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
The Company of Biologists
2016-08-01
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| Series: | Disease Models & Mechanisms |
| Assuntos: | |
| Acceso en liña: | http://dmm.biologists.org/content/9/8/899 |
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