Literature DB >> 6106182

Defect in soluble tyrosine aminotransferase in skin fibroblasts of a patient with tyrosinemia.

G W deGroot, K Dakshinamurti, L Allan, J C Haworth.   

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Year:  1980        PMID: 6106182     DOI: 10.1203/00006450-198007000-00013

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


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  1 in total

1.  Increased prevalence of hereditary metabolic diseases among native Indians in Manitoba and northwestern Ontario.

Authors:  J C Haworth; L A Dilling; L E Seargeant
Journal:  CMAJ       Date:  1991-07-15       Impact factor: 8.262

  1 in total

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