NAGLU Mutations Underlying Sanfilippo Syndrome Type B-Reference-Cited by-同舟云学术

NAGLU Mutations Underlying Sanfilippo Syndrome Type B

Published:1998-01 Issue:1 Volume:62 Page:64-69
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Schmidtchen Artur,Greenberg David,Zhao Hong G.,Li Hong Hua,Huang Yan,Tieu Phuong,Zhao Hui-Zhi,Cheng Samson,Zhao Zhaoyang,Whitley Chester B.,Di Natale Paola,Neufeld Elizabeth F.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference16 articles.

1. Mutation analysis in Sanfilippo syndrome type B by automated sequencing of the NAGLU coding region;Aronovich;Am J Hum Genet,1996

2. 4-Methylumbelliferyl 2-acetamido-2-deoxy-α-D-glucopyranoside, a fluorogenic substrate for N-acetylglucosaminidase;Chow;Carbohydr Res,1981

3. Management of mucopolysaccharidosis type III;Cleary;Arch Dis Child,1993

4. 22 Genes from chromosome 17q21: cloning, sequencing, and characterization of mutations in breast cancer families and tumors;Friedman;Genomics,1995

5. Overexpression of the human lysosomal enzyme α-L-iduronidase in Chinese hamster ovary cells;Kakkis;Protein Expr Purif,1994

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