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Keyword [Familial amyloid polyneuropathy]
Result: 1 - 8 | Page: 1 of 1
1.
The Clinical, Pathological And Molecular Studies Of Familial Amyloid Polyneuropathy In China
2.
Study Of A Family With A Thr69Ala Mutation Of TTR Gene In Familial Amyloid Polyneuropathy Disease
3.
Research Of Transthyretin Gene Polymorphism And Clinical, Histopathological Features Of Familial Amyloid Polyneuropathy
4.
Characteristics Of Symptoms And TTR Mutations In Chinese FAP Patients
5.
The Study Of TTR Gly83Arg Mutation In A Chinese Family With Familial Amyloid Polyneuropathy
6.
The Molecular Mechanism Of Transhyretin Tryosine Nitration Participating In Amyloidosis With FAP Patients
7.
A Case Of Transthyretin-type Familial Amyloid Polyneuropathy Caused By F84S And Reported Cases Retrospective Analysis
8.
Analysis Of One Familiar Amyloid Polyneuropathy Family With Ocular Abnormalities And Induced By TTR Gene Glu74Lys Mutation
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