Malattia di Austin (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Malattia di Austin" in Italian language version.

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Burk, R, D Valle, GH Thomas, C Miller, A Moser, H Moser e KN Rosenbaum, Early manifestations of multiple sulfatase deficiency†, in The Journal of Pediatrics, vol. 104, n. 4, 1984, pp. 574, DOI:10.1016/S0022-3476(84)80550-8, PMID 6142938.

Dierks, T; Schmidt, B; Borissenko, Lv; Peng, J; Preusser, A; Mariappan, M; Von, Figura, K, Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme, in Cell, vol. 113, n. 4, maggio 2003, pp. 435–44, DOI:10.1016/S0092-8674(03)00347-7, PMID 12757705.
Schmidt, B; Selmer, T; Ingendoh, A; Von, Figura, K, A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency, in Cell, vol. 82, n. 2, luglio 1995, pp. 271–8, DOI:10.1016/0092-8674(95)90314-3, PMID 7628016.
Soong BW, Casamassima AC, Fink JK, Constantopoulos G, Horwitz AL, Multiple sulfatase deficiency, in Neurology, vol. 38, n. 8, 1988, pp. 1273–5, PMID 2899861.
Farooqui AA, Horrocks LA, Biochemical aspects of globoid and metachromatic leukodystrophies, in Neurochem Pathol, vol. 2, n. 3, 1984, pp. 189–218, DOI:10.1007/BF02834352, PMID 6152665.
Burk, R, D Valle, GH Thomas, C Miller, A Moser, H Moser e KN Rosenbaum, Early manifestations of multiple sulfatase deficiency†, in The Journal of Pediatrics, vol. 104, n. 4, 1984, pp. 574, DOI:10.1016/S0022-3476(84)80550-8, PMID 6142938.