Mutational Analysis of EXT1in a Chinese Family Affected by Hereditary Multiple Osteochondroma

OBJECTIVES: To discuss the mutational features and their relationships with disease in a family with hereditary multiple osteochondroma (HMO) from Guangxi Province (GXBB-1 family), China. METHODS: Genomic DNA and total mRNA were extracted from peripheral blood cells of GXBB-1 family members. Whole e...

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Detalles Bibliográficos
Autores principales: Yuan, Guangzhi, Su, Qiang, Liao, Wenjun, Hou, Wei, Huang, Linke, Wang, Peng, Wu, Huayu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367584/
https://www.ncbi.nlm.nih.gov/pubmed/34409107
http://dx.doi.org/10.1155/2021/8888948

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367584/
https://www.ncbi.nlm.nih.gov/pubmed/34409107
http://dx.doi.org/10.1155/2021/8888948

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