Literature DB >> 930931

Adenosine deaminase deficiency: another family with "silent" ADA allele and normal ADA activity in two heterozygotes.

S H Chen, C R Scott, E R Giblett, A S Levin.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1977        PMID： 930931      PMCID： PMC1685505     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


× No keyword cloud information.
  4 in total

1.  Adenosine deaminase: demonstration of a "silent" gene associated with combined immunodeficiency disease.

Authors:  S H Chen; R Scott; E R Giblett
Journal:  Am J Hum Genet       Date:  1974-01       Impact factor: 11.025

2.  A new allele in red cell adenosine deaminase polymorphism: ADA.

Authors:  B Brinkmann; M Brinkmann; H Martin
Journal:  Hum Hered       Date:  1973       Impact factor: 0.444

Review 3.  Defects of purine metabolism in immunodeficiency diseases.

Authors:  R Hirschhorn
Journal:  Prog Clin Immunol       Date:  1977

4.  A normal level of adenosine deaminase activity in the red cell lysates of carriers and patients with severe combined immunodeficiency disease.

Authors:  P P Trotta; E M Smithwick; M E Balis
Journal:  Proc Natl Acad Sci U S A       Date:  1976-01       Impact factor: 11.205
  4 in total
  1 in total

1.  Heterozygote expression in propionyl coenzyme A carboxylase deficiency. Differences between major complementation groups.

Authors:  B Wolf; L E Rosenberg
Journal:  J Clin Invest       Date:  1978-11       Impact factor: 14.808
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.