Lysosomal alpha-N-acetylgalactosaminidase deficiency: a new inherited metabolic disease.

Authors	O P van Diggelen, D Schindler, W J Kleijer, J M Huijmans, H Galjaard, H U Linden, J Peter-Katalinic, H Egge, U Dabrowski, M Cantz
Journal	Lancet (London, England) (Lancet) Vol. 2 Issue 8562 Pg. 804 (Oct 03 1987) ISSN: 0140-6736 [Print] England
PMID	2889023 (Publication Type: Case Reports, Letter)
Chemical References	Hexosaminidases NAGA protein, human alpha-N-Acetylgalactosaminidase
Topics	Carbohydrate Metabolism, Inborn Errors (genetics) Child, Preschool Hexosaminidases (deficiency) Humans Male alpha-N-Acetylgalactosaminidase

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