A birth of bipartite exon by intragenic deletion

BACKGROUND: Disease‐causing mutations that activate transposon‐derived exons without creating a new splice‐site consensus have been reported rarely, but they provided unique insights into our understanding of structural motifs required for inclusion of intronic sequences in mature transcripts. METHO...

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Vydáno v:Mol Genet Genomic Med
Hlavní autoři: Nozu, Kandai, Iijima, Kazumoto, Igarashi, Toru, Yamada, Shiro, Kralovicova, Jana, Nozu, Yoshimi, Yamamura, Tomohiko, Minamikawa, Shogo, Morioka, Ichiro, Ninchoji, Takeshi, Kaito, Hiroshi, Nakanishi, Koichi, Vorechovsky, Igor
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2017
Témata:
Clinical Reports
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5441408/
https://ncbi.nlm.nih.gov/pubmed/28546999
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.277
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