Novel UBA Domain Mutations of SQSTM1 in Paget's Disease of Bone: Genotype Phenotype Correlation, Functional Analysis, and Structural Consequences-Reference-Cited by-同舟云学术

Novel UBA Domain Mutations of SQSTM1 in Paget's Disease of Bone: Genotype Phenotype Correlation, Functional Analysis, and Structural Consequences

Published:2004-03-22 Issue:7 Volume:19 Page:1122-1127
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Hocking Lynne J,Lucas Gavin JA,Daroszewska Anna,Cundy Tim,Nicholson Geoff C,Donath Judit,Walsh John P,Finlayson Catriona,Cavey James R,Ciani Barbara,Sheppard Paul W,Searle Mark S,Layfield Robert,Ralston Stuart H

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference18 articles.

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2. Familial aggregation of Paget's disease of bone;Siris;J Bone Miner Res,1991

3. A family study of Paget's disease of bone;Sofaer;J Epidemiol Community Health,1983

4. Genetic linkage of familial expansile osteolysis to chromosome 18q;Hughes;Hum Mol Genet,1994

5. Paget's disease of bone: Evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity;Haslam;J Bone Miner Res,1998

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