Literature DB >> 8017994

New method for detection of C34-T mutation in the AMPD1 gene causing myoadenylate deaminase deficiency.

M Gross.   

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Year:  1994        PMID： 8017994      PMCID： PMC1005342          DOI： 10.1136/ard.53.5.353

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN： 0003-4967            Impact factor:   19.103


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  2 in total

1.  Molecular basis of AMP deaminase deficiency in skeletal muscle.

Authors:  T Morisaki; M Gross; H Morisaki; D Pongratz; N Zöllner; E W Holmes
Journal:  Proc Natl Acad Sci U S A       Date:  1992-07-15       Impact factor: 11.205

2.  Characterization of the human and rat myoadenylate deaminase genes.

Authors:  R L Sabina; T Morisaki; P Clarke; R Eddy; T B Shows; C C Morton; E W Holmes
Journal:  J Biol Chem       Date:  1990-06-05       Impact factor: 5.157
  2 in total
  1 in total

Review 1.  Clinical heterogeneity and molecular mechanisms in inborn muscle AMP deaminase deficiency.

Authors:  M Gross
Journal:  J Inherit Metab Dis       Date:  1997-06       Impact factor: 4.982
  1 in total

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