Segregation within a family of two mutant alleles for hexosaminidase A-Reference-Cited by-同舟云学术

Segregation within a family of two mutant alleles for hexosaminidase A

Published:2008-04-23 Issue:5 Volume:9 Page:540-543
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Kelly Thaddeus E.,Reynolds Linda W.,O'Brien John S.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1976.tb01609.x/fullpdf

Reference7 articles.

1. Tay-Sachs disease: High gene frequency in a cox-Jewish population;Kelly;Amer. J. hum. Genet.,1975

2. Apparent deficiency of hexosaminidase A in healthy members of a family with Tay-Sachs disease;Navon;Amer. J. hum. Genet.,1973

3. O, Brien , J. S. A. G. W. Norden A. L. Miller R. G. Frost C. R. Scott J. Vidgoff T. E. Kelly 1976 Ganglioside GM 2 N-acetyl-β-D-galactosaminidase and asialo GM 2 (GA 2 ) N-acetyl-β-D-galactosaminidase: Studies in human skin fibroblasts Arch. Biochem. Biophys.

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