Literature DB >> 1861454

Galactose increase in an infant whose mother is heterozygous for peripheral uridine diphosphate galactose-4-epimerase deficiency.

K M Keller1, S Wirth, A C Sewell, Y S Shin.   

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Year:  1991        PMID： 1861454     DOI： 10.1007/bf01804403

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  2 in total

1.  A NEW METHOD FOR THE DETECTION OF GALACTOXEMIA AND ITS CARRIER STATE.

Authors:  E BEUTLER; M BALUDA; G N DONNELL
Journal:  J Lab Clin Med       Date:  1964-10

2.  Galactose-1-phosphate uridyl transferase deficiency due to Duarte/galactosemia combined variation: clinical and biochemical studies.

Authors:  H L Levy; S J Sepe; D S Walton; V E Shih; G Hammersen; S Houghton; E Beutler
Journal:  J Pediatr       Date:  1978-03       Impact factor: 4.406
  2 in total

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