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ERC-200044138
ERC-200044138
http://dx.doi.org/10.1081/ERC-200044138
The triple A syndrome is due to mutations in ALADIN, a novel member of the nuclear pore complex
P356
Q28303887-2E383A4F-25CB-442C-B246-77F8BC163278
P356
ERC-200044138
http://dx.doi.org/10.1081/ERC-200044138