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A lysosomal storage disorder in mice characterized by a dual deficiency of sphingomyelinase and glucocerebrosidase

✍ Scribed by P.G. Pentchev; A.E. Gal; A.D. Booth; F. Omodeo-Sale; J. Fours; B.A. Neumeyer; J.M. Quirk; G. Dawson; R.O. Brady

No coin nor oath required. For personal study only.

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