I-cell disease and pseudo-Hurler polydystrophy: heterozygote detection and characteristics of the altered N-acetyl-glucosamine-phosphotransferase in genetic variants.

Source:http://linkedlifedata.com/resource/pubmed/id/2998644

Clin. Chim. Acta 1985 Aug 30 150 3 175-83

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PMID
2998644