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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Kikuchi, H, Takata, A, Akasaka, Y, Fukuzawa, R, Yoneyama, H, Kurosawa, Y, Honda, M, Kamiyama, Y, Hata, J
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: 1998
विषय:
Research Article
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051186/
https://ncbi.nlm.nih.gov/pubmed/9475094
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