Molecular mechanisms leading to three different phenotypes in the cblD defect of intracellular cobalamin metabolism

Author: Stucki Martin   Coelho David   Suormala Terttu   Burda Patricie   Fowler Brian   Baumgartner Matthias R.  

Publisher: Oxford University Press

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.21, Iss.6, 2012-03, pp. : 1410-1418

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