Experts has a new look! Let us know what you think of the updates.

Provide feedback
Home
Scholarly Works
Novel point mutations in GDF5 associated with two...
Journal article

Novel point mutations in GDF5 associated with two distinct limb malformations in Chinese: brachydactyly type C and proximal symphalangism

Abstract

Growth/differentiation factor 5 (GDF5) is a secreted growth factor that plays a key regulatory role in embryonic skeletal and joint development. Mutations in the GDF5 gene can cause different types of skeletal dysplasia, including brachydactyly type C (BDC) and proximal symphalangism (SYM1). We report two novel mutations in the GDF5 gene in Chinese families with distinct limb malformations. In one family affected with BDC, we identified a novel …

Authors

Yang W; Cao L; Liu W; Jiang L; Sun M; Zhang D; Wang S; Lo WHY; Luo Y; Zhang X

Journal

Journal of Human Genetics, Vol. 53, No. 4, pp. 368–374

Publisher

Springer Nature

Publication Date

4 2008

DOI

10.1007/s10038-008-0253-7

ISSN

1434-5161