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Dive into the research topics of 'ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations'. Together they form a unique fingerprint.- Sort by
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Stephan Kemp, Aurora Pujol, Hans R. Waterham, Björn M. Van Geel, Corinne D. Boehm, Gerald V. Raymond, Garry R. Cutting, Ronald J.A. Wanders, Hugo W. Moser
Research output: Contribution to journal › Review article › peer-review