Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees-Reference-Cited by-同舟云学术

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Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees

Published:2004-07 Issue:1 Volume:35 Page:277-282
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Good David A,Busfield Frances,Fletcher Barbara H,Lovelock Paul K,Duffy David L,Kesting Janine B,Andersen John,Shaw Joanne T.E

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference29 articles.

1. Paget's disease of bone;Siris;J. Bone Miner. Res.,1998

2. Paget's disease of bone;Siris,1996

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

4. Frequency and characteristics of familial aggregation of paget's disease of bone;Morales-Piga;J. Bone Miner. Res.,1995

5. Evidence for linkage between HLA and paget's disease;Fotino;Transplant. Proc.,1977

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1. Diagnosis and treatment of Paget’s disease of bone: position paper from the Italian Society of Osteoporosis, Mineral Metabolism and Skeletal Diseases (SIOMMMS);Journal of Endocrinological Investigation;2024-03-15

2. Update on the pathogenesis and genetics of Paget’s disease of bone;Frontiers in Cell and Developmental Biology;2022-08-12

3. Clinical and Genetic Advances in Paget’s Disease of Bone: a Review;Clinical Reviews in Bone and Mineral Metabolism;2016-12-19

4. Hereditary Disorders of the Skeleton;Endocrinology: Adult and Pediatric;2016

5. Paget’s Disease;Pathobiology of Human Disease;2014

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