| 1 | APOA1, NNHA
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| Hereditary systemic amyloidosis with renal involvement.
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| Hawkins PN.
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| J Nephrol 16(3):443-8. Review.
2003
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| 2 | APOA1, NNHA
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| Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis.
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| Lachmann HJ, Booth DR, Booth SE, Bybee A, Gilbertson JA, Gillmore JD, Pepys MB, Hawkins PN.
|
| N Engl J Med 346(23):1786-91. 2002
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| 3 | APOA1, LAMP2, MEAX, NNHA
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| The new apolipoprotein A-I variant leu(174) --> Ser causes hereditary cardiac amyloidosis, and the amyloid fibrils are constituted by the 93-residue N-terminal polypeptide.
|
| Obici L, Bellotti V, Mangione P, Stoppini M, Arbustini E, Verga L, Zorzoli I, Anesi E, Zanotti G, Campana C, Viganò M, Merlini G.
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| Am J Pathol 155(3):695-702. 1999
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| 4 | APOA1, NNHA
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| Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene.
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| Booth DR, Tan SY, Booth SE, Tennent GA, Hutchinson WL, Hsuan JJ, Totty NF, Truong O, Soutar AK, Hawkins PN, Bruguera M, Caballería J, Solé M, Campistol JM, Pepys MB.
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| J Clin Invest 97(12):2714-21. 1996
|