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About this Biochemistry, Genetics and Molecular Biology article
Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease by L Michel-Calemard; F Dijoud; M Till; JC Lambert; M Vercherat; V Tardy; C Coubes; Y Morel is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- L Michel-Calemard; F Dijoud; M Till; JC Lambert; M Vercherat; V Tardy; C Coubes; Y Morel
- Publisher
- John Wiley and Sons; Wiley (Blackwell Publishing); Blackwell Publishing Inc.; Wiley (ISSN 0009-9163)
- Published
- 2009
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)