TBX6Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis
Author(s) -
Nan Wu,
Ming Xuan,
Jianqiu Xiao,
Zhihong Wu,
Xiaoli Chen,
Marwan Shinawi,
Joseph Shen,
Gaobo Yu,
Jiaqi Liu,
Hua Xie,
Zoran Gucev,
Shiyuan Liu,
Ni Yang,
Hussam AlKateb,
Jin Chen,
Jian Zhang,
Nik Hauser,
T Zhang,
Velibor Tasić,
P Liu,
Lei Su,
Xiaodong Pan,
Chunyu Liu,
L Wang,
Jianxiong Shen,
Y Chen,
Kwong Wai Choy,
Jin Wang,
Q Wang,
Shihua Li,
Weichen Zhou,
J. Guo,
Yipeng Wang,
C Zhang,
Hong Zhao,
Yu An,
Yu Zhao,
Zhihong Liu,
Yueming Zuo,
Yun Tian,
Xisheng Weng,
V. Reid Sutton,
H Wang,
Yulong Ming,
S Kulkarni,
Tao P. Zhong,
Philip F. Giampietro,
Sally L. Dunwoodie,
Sau Wai Cheung,
X Zhang,
Jin Li,
James R. Lupski,
Guixing Qiu,
Feng Zhang
Publication year - 2015
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1406829
Subject(s) - null allele , allele , congenital scoliosis , genetics , scoliosis , biology
Congenital scoliosis is a common type of vertebral malformation. Genetic susceptibility has been implicated in congenital scoliosis.
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