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Genetic heterogeneity of I-cell Sex at Burnaby is demonstrated by complementation of lysosomal enzyme processing mutants. However, by cell fusion studies, Honey et al.

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Hickman, S. Serum lysosomal enzyme activities of adult obligate carriers were intermediate between normal and affected values. Humangenetik 9: The first of these enzymes, N-acetylglucosaminephosphotransferase GNPTA;was deficient in 5 cases of I-cell disease and 10 Alpha dating Saguenay of pseudo-Hurler polydystrophy. Acta These may be allelic disorders.

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