Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis (Q24561552)
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(P1476) "Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis" (language: en)
(P2093) S Brul
A Westerveld
A Strijland
R J Wanders
A W Schram
H S Heymans
R B Schutgens
H van den Bosch
J M Tager
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