Literature DB >> 924442

Familial incidence of L-xylulosuria.

O S Reddi, S V Reddy, K R Reddy.   

Abstract

During a survey for genetic disorders, L-Xylulosuria, an autosomal recessive condition, was found to affect three cousins in an inbred family. There were no clinical symptoms.

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Year:  1977        PMID: 924442     DOI: 10.1007/bf00273166

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  7 in total

1.  Specific determination of blood glucose with o-toluidine.

Authors:  A HYVARINEN; E A NIKKILA
Journal:  Clin Chim Acta       Date:  1962-01       Impact factor: 3.786

2.  A sensitive and stereospecific enzymatic assay for xylulose.

Authors:  J HICKMAN; G ASHWELL
Journal:  J Biol Chem       Date:  1959-04       Impact factor: 5.157

3.  Essential pentosuria.

Authors:  A K KHACHADURIAN
Journal:  Am J Hum Genet       Date:  1962-09       Impact factor: 11.025

4.  The inheritance of essential pentosuria.

Authors:  P D ROBERTS
Journal:  Br Med J       Date:  1960-05-14

5.  L-xylulosuria in a Lebanese family.

Authors:  W M POLITZER; H FLEISCHMANN
Journal:  Am J Hum Genet       Date:  1962-09       Impact factor: 11.025

6.  The enzymatic defect in essential pentosuria.

Authors:  Y M Wang; J Van Eys
Journal:  N Engl J Med       Date:  1970-04-16       Impact factor: 91.245

7.  Inbreeding in India.

Authors:  L D Sanghvi
Journal:  Eugen Q       Date:  1966-12
  7 in total

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