The molecular basis of transferase galactosaemia in South African negroids-Reference-Cited by-同舟云学术

The molecular basis of transferase galactosaemia in South African negroids

Published:1999-02 Issue:1 Volume:22 Page:37-42
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Manga N.¹,Jenkins T.¹,Jackson H.¹,Whittaker D. A.¹,Lane A. B.¹

Affiliation:

1. ; Department of Human Genetics, School of Pathology; The South African Institute for Medical Research and the University of the Witwatersrand; Johannesburg South Africa

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005491014280/fullpdf

Reference16 articles.

1. New rapid method for the estimation of red cell galactose-1-phosphate uridyltransferase activity;Beutler;Lab Clin Med,1968

2. A common mutation associated with the Duarte allele;Elsas;Am J Hum Genet,1994

3. Identification and functional analysis of three distinct mutations in the human galactose-1-phosphate uridyltransferase gene associated with galactosemia in a single family;Fridovich-Keil;Am J Hum Genet,1995

4. Regional mapping of GALT on the short arm of chromosome 9;Kondo;Cytogenet Cell Genet,1984

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