A new from of residual hexosaminidase activity in infantile Tay Sachs disease fibroblasts-Reference-Cited by-同舟云学术

A new from of residual hexosaminidase activity in infantile Tay Sachs disease fibroblasts

Published:2008-06-28 Issue:3 Volume:24 Page:206-215
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Hechtman P.,Khoo K.,Isaacs C.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1983.tb02241.x/fullpdf

Reference27 articles.

1. Anderman , E. C. R. Scriver L. S. Wolfe L. Dansky F. Anderman 1977 Genetic variants of Tay-Scahs Disease and Sandhoff's Disease: and Sandhoff's Disease in French-Canadians, Juvenlie Tay Scachs Disease in Lebabease Canadians, and a Tay-Sachs screening program in the French-Canadian population Prog. Clin. Biol. Res. 161 188

2. Non-enzymic conversion of human hexosaminidase;Beulter;J. Lab. Clin. Med.,1975a

3. Hexosaminidase isozymes in Type 0 Gm2 Gangliosidosis (Sandhoff-Jatzkewitz Disease);Beuler;Amer J. hum. Genet.,1975b

4. Studies on human β-D-N-Acetylhexosaminidases C separated from neonatal brain;Besley;Biochem. J.,1976

5. Separation and properties of human brain hexosaminidase;Braidman;C. Biochem. J.,1974

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1. Microheterogeneity of Serum β-Hexosaminidase in Chronic Alcohol Abusers in a Driver's License Regranting Program;Alcoholism: Clinical and Experimental Research;2013-04-23

2. A deletion involving Alu sequences in the beta-hexosaminidase alpha-chain gene of French Canadians with Tay-Sachs disease.;Journal of Biological Chemistry;1987-11

3. N-Acetyl-β-hexosaminidase B deficiency in cultured fibroblasts from a patient with progressive motor neuron disease;Biochemical and Biophysical Research Communications;1985-08