Acid sphingomyelinase deficiency. Phenotype variability with prevalence of intermediate phenotype in a series of twenty‐five Czech and Slovak patients. A multi‐approach study von Pavlů‐Pereira, H., Asfaw, B., Poupčtová, H., Ledvinová, J., Sikora, J., Vanier, M. T., Sandhoff, K., Zeman, J., Novotná, Z., Chudoba, D., Elleder, M.

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