Literature DB >> 6093679

DNA analysis in patients with hereditary fructose intolerance.

C Grégori, C Besmond, M Odievre, A Kahn, J C Dreyfus.   

Abstract

Restriction fragments of the aldolase B gene were studied in 11 patients with hereditary fructose intolerance and compared with the normal pattern. No major deletion of the gene was observed. One patient was found to be a compound heterozygote since one allele with normal restriction sites was inherited from the mother and the other with an abnormal Bam HI site was inherited from the father. The anomaly of the Bam HI fragment observed in this family was not found in 62 normal controls from the same origin as the patient.

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Year:  1984        PMID: 6093679     DOI: 10.1111/j.1469-1809.1984.tb00842.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  4 in total

1.  Partial aldolase B gene deletions in hereditary fructose intolerance.

Authors:  N C Cross; T M Cox
Journal:  Am J Hum Genet       Date:  1990-07       Impact factor: 11.025

2.  Mapping of a restriction fragment length polymorphism within the human aldolase B gene.

Authors:  G Paolella; R Santamaria; P Buono; F Salvatore
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

Review 3.  Diagnosis of genetic disease using recombinant DNA.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1986-05       Impact factor: 4.132

4.  Molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). RNA and DNA analysis.

Authors:  S Gautron; D Daegelen; F Mennecier; D Dubocq; A Kahn; J C Dreyfus
Journal:  J Clin Invest       Date:  1987-01       Impact factor: 14.808

  4 in total

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