Fibroblasts From Patients With I-Cell Disease and Pseudo-Hurler Polydystrophy Are Deficient in Uridine 5'-Diphosphate-N-Acetylglucosamine: Glycoprotein N-Acetylglucosaminylphosphotransferase Activity.

Journal of Clinical Investigation - United States
doi 10.1172/jci110189
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American Society for Clinical Investigation

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