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Mutation in PEX16 Is Causal in the Peroxisome-Deficient Zellweger Syndrome of Complementation Group D
Masanori Honsho, Shigehiko Tamura, Nobuyuki Shimozawa, Yasuyuki Suzuki, Naomi Kondo, Yukio FujikiVolume:
63
Year:
1998
Language:
english
DOI:
10.1086/302161
File:
PDF, 535 KB
english, 1998