Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7)-Reference-Cited by-同舟云学术

Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7)

Published:2020-08 Issue: Volume:137 Page:115364
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Whyte Michael P.,Campeau Philippe M.^ORCID,McAlister William H.,Roodman G. David,Kurihara Nori,Nenninger Angela,Duan Shenghui,Gottesman Gary S.,Bijanki Vinieth N.,Sedighi Homer,Veis Deborah J.,Mumm Steven

Funder

Shriners Hospitals for Children

Barnes-Jewish Hospital Foundation

Fonds de Recherche du Québec - Santé

Canadian Institutes of Health Research

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference58 articles.

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3. Bone Dysplasias: An Atlas of Genetic Disorders of Skeletal Development,2002

4. Osteoprotegerin deficiency and juvenile Paget's disease;Whyte;N. Engl. J. Med.,2002

5. Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/ NF-κB signaling;Whyte;Ann. N. Y. Acad. Sci.,2006

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