(Q55417076)
Statements
Prosaposin deficiency and saposin B deficiency (activator-deficient metachromatic leukodystrophy): report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutations (English)
Helena Mysková
Milan Elleder
Margret Petermöller
Heidi Mayrhofer
Martin Staudt
Barbara C Paton
Klaus Harzer
Ingeborg Krägeloh-Mann
1 February 2009
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