Gene mutations in sporadic lymphangioleiomyomatosis and genotype–phenotype correlation analysis

BACKGROUND: Sporadic lymphangioleiomyomatosis (S-LAM) is a rare neoplasm with heterogeneous clinical features that is conventionally considered to be related to TSC2. This study serves to elucidate the mutation landscape and potential correlation between S-LAM genomic profiles and clinical phenotype...

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Detalles Bibliográficos
Autores principales: Huang, Jiannan, Xu, Wenshuai, Liu, Peng, Liu, Yaping, Shen, Cheng, Liu, Song, Wang, Yani, Wang, Jun, Zhang, Tengyue, He, Yudi, Cheng, Chongsheng, Yang, Luning, Zhang, Weihong, Tian, Xinlun, Xu, Kai-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482747/
https://www.ncbi.nlm.nih.gov/pubmed/36117164
http://dx.doi.org/10.1186/s12890-022-02154-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482747/
https://www.ncbi.nlm.nih.gov/pubmed/36117164
http://dx.doi.org/10.1186/s12890-022-02154-0

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