Genotype-phenotype analysis of F-helix mutations at the kinase domain of TGFBR2, including a type 2 Marfan syndrome familial study

PURPOSE: Transforming growth factor beta receptor II (TGFBR2) gene mutations are associated with Marfan syndrome; however, the relationship between the mutations and clinical phenotypes are not clear. METHODS: Genomic DNA from peripheral blood leukocytes of a Chinese proband with Marfan syndrome, fi...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Lin, Gao, Ling-Gen, Zhang, Ming, Zhou, Xian-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258522/
https://www.ncbi.nlm.nih.gov/pubmed/22259224

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258522/
https://www.ncbi.nlm.nih.gov/pubmed/22259224

Ejemplares similares