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Gene Review

KIAA0319L  -  KIAA0319-like

Homo sapiens

Synonyms: Dyslexia-associated protein KIAA0319-like protein, KIAA1837, PP791
 
 
 
 
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Biological context of KIAA0319L

  • Studies elsewhere have suggested that gene conversion may be a significant cause of mutation at PKD1, but only 3 of 69 different mutations matched PKD1-like HG sequence [1].

References

  1. Mutation analysis of the entire PKD1 gene: genetic and diagnostic implications. Rossetti, S., Strmecki, L., Gamble, V., Burton, S., Sneddon, V., Peral, B., Roy, S., Bakkaloglu, A., Komel, R., Winearls, C.G., Harris, P.C. Am. J. Hum. Genet. (2001) [Pubmed]
 
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