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Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene.
Booth, David R.; Tan, Si-Yen; Booth, Sussanne E.; Tennent, Glenys A.; Hutchinson, Winston L.; Hsuan, J. Justin; Totty, Nicholas F.; Truong, Oanh; Soutar, Anne K.; Hawkins, Philip N.; Bruguera i Cortada, Miquel, 1942-; Caballeria Rovira, Joan; Solé, Manel; Campistol Plana, Josep M.; Pepys, Mark B.
Universitat de Barcelona
2010-05-04
Amiloïdosi
Proteïnes
Fetge
Genètica molecular
Amyloidosis
Apolipoprotein AI
Gene
Liver
Mutation
(c) The American Society for Clinical Investigation, 1996
Article
American Society for Clinical Investigation
         

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Booth, David R.; Tan, Si-Yen; Booth, Sussanne E.; Tennent, Glenys A.; Hutchinson, Winston L.; Hsuan, J. Justin; Totty, Nicholas F.; Truong, Oanh; Soutar, Anne K.; Hawkins, Philip N.; Bruguera i Cortada, Miquel, 1942-; Caballeria Rovira, Joan; Solé, Manel; Campistol Plana, Josep M.; Pepys, Mark B.
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