2023
DOI: 10.1016/j.lpm.2023.104170
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Alpha1-antitrypsin deficiency: An updated review

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(1 citation statement)
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“…Alpha-1 antitrypsin deficiency models Alpha-1 antitrypsin (AAT) deficiency is a condition characterized by a lack of AAT due to mutations in the SERPINA1 gene [81,82]. More than 90% of severe deficiency patients are homozygous for Z (Glu342Lys) mutation.…”
Section: Monogenic Liver Disease Modelsmentioning
confidence: 99%
“…Alpha-1 antitrypsin deficiency models Alpha-1 antitrypsin (AAT) deficiency is a condition characterized by a lack of AAT due to mutations in the SERPINA1 gene [81,82]. More than 90% of severe deficiency patients are homozygous for Z (Glu342Lys) mutation.…”
Section: Monogenic Liver Disease Modelsmentioning
confidence: 99%