TNFRSF11A GENE ALLELIC VARIANTS ARE ASSOCIATED WITH PAGET'S DISEASE OF BONE AND INTERACT WITH SQSTM1 MUTATIONS TO CAUSE THE SEVERITY OF THE DISORDER

被引：0

作者：

Merlotti, Daniela ^{[1
]}

Formicola, Daniela ^{[5
]}

Mingione, Alessandra ^{[5
]}

Fenoglio, Pierpaola ^{[4
]}

Criasia, Antonio ^{[3
]}

Muscariello, Riccardo ^{[2
]}

Strazzullo, Pasquale ^{[2
]}

Isaia, Giancarlo ^{[3
]}

Layfield, Robert ^{[6
]}

Nuti, Ranuccio ^{[1
]}

Gianfrancesco, Fernando ^{[5
]}

Gennari, Luigi ^{[1
]}

Rendina, Domenico ^{[2
]}

Di Stefano, Marco ^{[3
]}

Mossetti, Giuseppe ^{[2
]}

Gallone, Salvatore ^{[4
]}

Esposito, Teresa ^{[5
]}

Magliocca, Sara ^{[5
]}

Goode, Alice ^{[6
]}

机构：

[1] Univ Siena, Dept Internal Med Endocrine Metab Sci & Biochem, I-53100 Siena, Italy

[2] Univ Naples Federico 2, Sch Med, Dept Clin & Expt Med, Naples, Italy

[3] Univ Turin, Dept Med & Surg Sci, Geriatr Sect, Turin, Italy

[4] Univ Turin, Dept Neurosci, Turin, Italy

[5] CNR, Inst Genet & Biophys, I-80125 Naples, Italy

[6] Univ Nottingham, Sch Med, Queens Med Ctr, Sch Biomed Sci, Nottingham, England

来源：

OSTEOPOROSIS INTERNATIONAL | 2011年 / 22卷

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：14 / 15

页数：2

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[1] TNFRSF11A GENE ALLELIC VARIANTS ARE ASSOCIATED WITH PAGET'S DISEASE OF BONE AND INTERACT WITH SQSTM1 MUTATIONS TO CAUSE THE SEVERITY OF THE DISORDER
Merlotti, Daniela
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Mingione, Alessandra
Fenoglio, Pierpaola
Criasia, Antonio
Muscariello, Riccardo
Strazzullo, Pasquale
Isaia, Giancarlo
Layfield, Robert
Nuti, Ranuccio
Gianfrancesco, Fernando
Gennari, Luigi
Rendina, Domenico
Di Stefano, Marco
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[2] Mutations in the SQSTM1 gene are sufficient to cause Paget's disease of bone
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[5] Mutations of SQSTM1 strongly predict disease severity and complications in Paget's disease of bone
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[7] Pattern of SQSTM1 Gene Variants in a Hungarian Cohort of Paget’s Disease of Bone
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[8] Absence of Somatic SQSTM1 Mutations in Paget's Disease of Bone
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[10] SQSTM1 and Paget's disease of bone
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