Precise detection of a murine germline mutation of the Notch3 gene associated with kyphosis and developmental disorders

Journal of Advanced Veterinary and Animal Research

Jianning Tao¹  Dakota L. Callahan²  Yuxia Cao³  Tania Rodezno-Antunes³  Ashley VanCleave³  Jennifer J. Westendorf⁴  Haydee M. Torres⁵ 

[1] Cancer Biology & Rare Diseases Groups, Sanford Research, Sioux Falls, SD, USA. & Department of Chemistry & Biochemistry, The South Dakota State University, Brookings, SD, USA. & Department of Biomedical Engineering, the University of South Dakota, Sioux Falls, SD, USA. & Department of Pediatrics the University of South Dakota, Sioux Falls, SD, USA.;Cancer Biology & Rare Diseases Groups, Sanford Research, Sioux Falls, SD, USA. & Sanford Program for Undergraduate Research, University of Sioux Falls, Sioux Falls, SD, USA;Cancer Biology & Rare Diseases Groups, Sanford Research, Sioux Falls, SD, USA;Department of Orthopedic Surgery, Mayo Clinic, Rochester, MN, USA;Cancer Biology & Rare Diseases Groups, Sanford Research, Sioux Falls, SD, USA. & Department of Chemistry & Biochemistry, The South Dakota State University, Brookings, SD, USA;

关键词: lateral meningocele syndrome;    notch3 mutation;    arms;    genotyping;    skeletal disease;   

DOI  :  10.5455/javar.2021.h479

来源: DOAJ

【 授权许可】

Unknown