Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease
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V. Tardy | Y. Morel | L. Michel-Calemard | F. Dijoud | M. Till | J. Lambert | M. Vercherat | C. Coubes | L. Michel‐Calemard | JC Lambert