Diagnosis of alpha-1-antitrypsin deficiency by DNA analysis of children with liver disease
Background - Alpha-1-antitrypsin deficiency is a genetic disorder which is transmitted in a co-dominant, autosomal form. Alpha-1-antitrypsin deficiency affects mainly the lungs and the liver leading, in the latter case, to neonatal cholestasis, chronic hepatitis or cirrhosis. A precise diagnosis of...
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| Outros Autores: | , , , , |
| Formato: | article |
| Idioma: | eng |
| Publicado em: |
2001
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| Texto completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-28032001000100012 |
| País: | Brasil |
| Oai: | oai:scielo:S0004-28032001000100012 |