Article Text
Articles
PiPclifton: a new α1-antitrypsin allele in an American Negro family
Abstract
Serum specimens from eight females and two males representing three generations of an American Negro family exhibited an α1-antitrypsin phenotype that we labelled MPclifton because of its electrophoretic mobility. The family study and examination of multiple specimens from the same subject indicated that the phenotype represented an α1-antitrypsin allele, labelled PiPclifton. The new genetic variant is not associated with deficiency of α1-antitrypsin or of trypsin inhibitory capacity in the serum.
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Footnotes
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↵* This work was supported by NIH Grants RR 005535 and RR 00123 and by the Children's Hospital Research Foundation.
Received for publication 6 March 1980