Comparative proteomics analysis for identifying the lipid metabolism related pathways in patients with Klippel-Feil syndrome

BACKGROUND: Klippel-Feil syndrome (KFS) represents the rare and complex deformity characterized by congenital defects in the formation or segmentation of the cervical vertebrae. There is a wide gap in understanding the detailed mechanisms of KFS because of its rarity, heterogeneity, small pedigrees,...

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Detalles Bibliográficos
Autores principales: Li, Ziquan, Zhang, Cong, Qiu, Bintao, Niu, Yuchen, Leng, Ling, Cai, Siyi, Tian, Ye, Zhang, Terry Jianguo, Qiu, Guixing, Wu, Nan, Wu, Zhihong, Wang, Yipeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940892/
https://www.ncbi.nlm.nih.gov/pubmed/33708882
http://dx.doi.org/10.21037/atm-20-5155

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940892/
https://www.ncbi.nlm.nih.gov/pubmed/33708882
http://dx.doi.org/10.21037/atm-20-5155

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