![](/img/cover-not-exists.png)
Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease
L Michel-Calemard, F Dijoud, M Till, JC Lambert, M Vercherat, V Tardy, C Coubes, Y MorelVolume:
75
Year:
2009
Language:
english
Pages:
4
DOI:
10.1111/j.1399-0004.2008.01106.x
File:
PDF, 262 KB
english, 2009