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niemann-pick disease, type b
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SMPD1
An MspI polymorphism in the human acid sphingomyelinase gene (SMPD1)
Molecular basis of acid sphingomyelinase deficiency in a patient with Niemann-Pick disease type A
Structural organization and complete nucleotide sequence of the gene encoding human acid sphingomyelinase (SMPD1)
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