Inherited human complement C5 deficiency. Nonsense mutations in exons 1 (Gln1 to Stop) and 36 (Arg1458 to Stop) and compound heterozygosity in three African-American families.

Source:http://linkedlifedata.com/resource/pubmed/id/7730648

J. Immunol. 1995 May 15 154 10 5464-71

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PMID
7730648