Literature DB >> 5555219

The third variant of human myoglobin showing an unusual amino acid substitution: 138(H16)arginine--tryptophan.

F E Boulton, R G Huntsman, A Romero Herrera, P A Lorkin, H Lehmann.   

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Year:  1971        PMID： 5555219     DOI： 10.1016/0005-2795(71)90288-1

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN： 0006-3002


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  1 in total

1.  Myoglobin in primary muscular disease. I. Duchenne muscular dystrophy. II. Muscular dystrophy of distal type.

Authors:  A E Romero-Herrera; H Lehmann; B E Tomlinson; J N Walton
Journal:  J Med Genet       Date:  1973-12       Impact factor: 6.318
  1 in total

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