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SAPA METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY PSAP SAP1, FORMERLY SAPC SAPOSIN C SAPOSIN A PARKINSON DISEASE 24, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY SPHINGOLIPID ACTIVATOR PROTEIN 2, FORMERLY SAPOSIN D SAPB SAPOSIN B COMBINED SAPOSIN DEFICIENCY SPHINGOLIPID ACTIVATOR PROTEIN 1, FORMERLY SAP2, FORMERLY SAPD
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