Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome?

The WT1 gene, one of the genes responsible for Wilms tumour, is thought to play a crucial role in the development of the kidneys and gonads. This gene encodes four protein isoforms resulting from two alternative splicing sites, one of which involves inclusion or exclusion of lysine, threonine, and s...

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Hlavní autoři: Kikuchi, H, Takata, A, Akasaka, Y, Fukuzawa, R, Yoneyama, H, Kurosawa, Y, Honda, M, Kamiyama, Y, Hata, J
Médium: Artigo
Jazyk:Inglês
Vydáno: 1998
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051186/
https://ncbi.nlm.nih.gov/pubmed/9475094
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