Molecular analysis of Paget's disease of bone

被引：0

作者：

Michou, L. ^{[1
]}

Collet, C. ^{[1
]}

Orcel, P. ^{[1
]}

机构：

[1] Hop Lariboisiere, Assistance Publ Hop Paris, Reseau Natl Genet Maladie Paget, Federat Rhumatol, F-75475 Paris, France

来源：

PATHOLOGIE BIOLOGIE | 2007年 / 55卷 / 3-4期

关键词：

Paget's disease of bone; sequestosomel; mutations; genetic testing;

D O I：

10.1016/j.patbio.2006.06.005

中图分类号：

R36 [病理学];

学科分类号：

100104 ;

摘要：

引用

页码：131 / 133

页数：3

共 6 条

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[2] Novel UBA domain mutations of SQSTM1 in Paget's disease of bone:: Genotype phenotype correlation, functional analysis, and structural consequences [J].

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[3] Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone [J].

Laurin, N ;

Brown, JP ;

Morissette, J ;

Raymond, V .

AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (06) :1582-1588

[4] Genetics of Paget's disease of bone [J].

Michou, L ;

Collet, C ;

Laplanche, JL ;

Orcel, P ;

Cornélis, F .

JOINT BONE SPINE, 2006, 73 (03) :243-248

[5]

MORALESPIGA AA, 1995, J BONE MINER RES, V10, P663

[6] Paget's disease of bone [J].

Siris, ES .

JOURNAL OF BONE AND MINERAL RESEARCH, 1998, 13 (07) :1061-1065

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