[The clinical significance of hereditary and acquired alpha-1-antitrypsin deficiency in patients with liver cirrhosis and Wilson-Konovalov disease]

Autor:	N A, Shaposhnikova, I S, Shuliat'ev, G G, Varvanina, V N, Drozdov
Rok vydání:	2011
Předmět:	Adult Liver Cirrhosis Male Polymorphism Genetic Middle Aged Polymerase Chain Reaction Hepatolenticular Degeneration Liver Function Tests Predictive Value of Tests Case-Control Studies alpha 1-Antitrypsin alpha 1-Antitrypsin Deficiency Chronic Disease Mutation Humans Female Copper
Zdroj:	Eksperimental'naia i klinicheskaia gastroenterologiia = Experimentalclinical gastroenterology. (10)
ISSN:	1682-8658
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::291014e25c941d1eead360990a7c56b9 https://pubmed.ncbi.nlm.nih.gov/21434364 Zobrazit plný text záznamu