(Q34997849)
Statements
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Genomic mutations associated with mild and severe deficiencies of transcobalamin I (haptocorrin) that cause mildly and severely low serum cobalamin levels (English)
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Ralph Carmel
1 reference
James Parker
1 reference
Zvi Kelman
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17 August 2009
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147
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3
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386-391
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Identifiers
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1 reference