Cloning of the human alpha 1 antichymotrypsin gene and genetic analysis of the gene in relation to alpha 1 antitrypsin deficiency.

Deficiency of alpha 1 antitrypsin (Pi) is clinically heterogeneous and the unpredictability of the clinical manifestation in a person of phenotype PiZ, which may vary from severe childhood liver disease to normal health, is a problem in genetic counselling. This problem may increase as couples at ri...

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Detalhes bibliográficos
Main Authors: Kelsey, G D, Abeliovich, D, McMahon, C J, Whitehouse, D, Corney, G, Povey, S, Hopkinson, D A, Wolfe, J, Mieli-Vergani, G, Mowat, A P
Formato: Artigo
Idioma:Inglês
Publicado em: 1988
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050502/
https://ncbi.nlm.nih.gov/pubmed/3260956
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