BGN Mutations in X-Linked Spondyloepimetaphyseal Dysplasia-Reference-Cited by-同舟云学术

BGN Mutations in X-Linked Spondyloepimetaphyseal Dysplasia

Published:2016-06 Issue:6 Volume:98 Page:1243-1248
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Cho Sung Yoon,Bae Jun-Seok,Kim Nayoung K.D.,Forzano Francesca,Girisha Katta Mohan,Baldo Chiara,Faravelli Francesca,Cho Tae-Joon,Kim Dongsup,Lee Kyoung Yeul,Ikegawa Shiro,Shim Jong Sup,Ko Ah-Ra,Miyake Noriko,Nishimura Gen,Superti-Furga Andrea,Spranger Jürgen,Kim Ok-Hwa,Park Woong-Yang,Jin Dong-Kyu

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference14 articles.

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4. Biglycan regulates the expression of EGF receptors through EGF signaling pathways in human articular chondrocytes;Iacob;Connect. Tissue Res.,2010

5. Targeted disruption of the biglycan gene leads to an osteoporosis-like phenotype in mice;Xu;Nat. Genet.,1998

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