The first pure form of Ostertag-type amyloidosis in Japan: a sporadic case of hereditary fibrinogen Aα-chain amyloidosis associated with a novel frameshift variant

被引：15

作者：

Yazaki, Masahide ^{[1
,2
]}

Yoshinaga, Tsuneaki ^{[2
]}

Sekijima, Yoshiki ^{[1
,2
]}

Nishio, Saori ^{[3
]}

Kanizawa, Yuji ^{[4
]}

Kametani, Fuyuki ^{[5
]}

Miyashita, Kana ^{[6
]}

Hachiya, Naomi ^{[6
]}

Higuchi, Keiichi ^{[1
,7
]}

Ikeda, Shu-ichi ^{[1
,2
]}

机构：

[1] Shinshu Univ, Inst Biomed Sci, Dept Biol Sci Intractable Neurol Disorders, Matsumoto, Nagano 390, Japan

[2] Shinshu Univ, Sch Med, Dept Med Neurol & Rheumatol, Matsumoto, Nagano 390, Japan

[3] Hokkaido Univ, Grad Sch Med, Div Rheumatol Endocrinol & Nephrol, Sapporo, Hokkaido, Japan

[4] Oji Gen Hosp, Dept Hematol, Tomakomai, Japan

[5] Tokyo Metropolitan Inst Med Sci, Tokyo 113, Japan

[6] Tokyo Med Univ, Dept Neurophysiol, Tokyo 1608402, Japan

[7] Shinshu Univ, Grad Sch Med, Inst Pathogenesis & Dis Prevent, Dept Aging Biol, Matsumoto, Nagano 390, Japan

来源：

AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS | 2015年 / 22卷 / 02期

关键词：

RENAL AMYLOIDOSIS; SHIFT MUTATION; GENE;

D O I：

10.3109/13506129.2015.1037389

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：142 / 144

页数：3

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