bibliographic entry 2441701 [be/2441701]
https://w3id.org/oc/corpus/be/2441701

is a
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  • Spiegel R, Bach G, Sury V, Mengistu G, Meidan B, Shalev S, Shneor Y, Mandel H, Zeigler M. 2005 A mutation in the saposin A coding region of the prosaposin gene in an infant presenting as Krabbe disease: first report of saposin A deficiency in humans. Mol Genet Metab 84: 160–166. PMID: 15773042
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