Literature DB >> 7318169

Detection of UDP-galactose-4-epimerase deficiency in a galactosemia screening program.

H Misumi, H Wada, M Kawakami, H Ninomiya, T Sueishi, Y Ichiba, T Shohmori.   

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Year:  1981        PMID： 7318169     DOI： 10.1016/0009-8981(81)90173-x

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN： 0009-8981            Impact factor:   3.786


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  3 in total

1.  Results of newborn screening for galactose metabolic disorders.

Authors:  B Inoue; M Hata; Y Ichiba; H Wada; H Misumi; T Mori
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Development of a protocol for newborn screening for disorders of the galactose metabolic pathway.

Authors:  F G Bowling; A R Brown
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

3.  Molecular characterization of a unique patient with epimerase-deficiency galactosaemia.

Authors:  A Alano; S Almashanu; J M Chinsky; P Costeas; M G Blitzer; E A Wulfsberg; T M Cowan
Journal:  J Inherit Metab Dis       Date:  1998-06       Impact factor: 4.982
  3 in total

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