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Molecular mechanisms leading to three different phenotypes in the cblD defect of intracellular cobalamin metabolismSTUCKI, Martin; COELHO, David; SUORMALA, Terttu et al.Human molecular genetics (Print). 2012, Vol 21, Num 6, pp 1410-1418, issn 0964-6906, 9 p.Article

Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B₁₂ metabolismRUTSCH, Frank; GAILUS, Susann; STUCKI, Martin et al.Nature genetics. 2009, Vol 41, Num 2, pp 234-239, issn 1061-4036, 6 p.Article

Gene Identification for the cblD Defect of Vitamin B₁₂ MetabolismCOELHO, David; SUORMALA, Terttu; STUCKI, Martin et al.The New England journal of medicine. 2008, Vol 358, Num 14, pp 1454-1464, issn 0028-4793, 11 p.Article