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Rare alpha 1 antitrypsin allele PI W and a history of infant liver disease

โœ Scribed by Clark, Dr. P. ;Chong, A. Y. H.


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
496 KB
Volume
45
Category
Article
ISSN
0148-7299

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In recent years, we have witnessed several important paradigm shifts in understanding the molecular basis of liver disease in alpha-1-antitrypsin (AT) deficiency. These shifts have become possible as a result of a number of advances in research on the cell biology of aggregation-prone mutant protein