Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma

PURPOSE: The LZTR1 gene has been associated with schwannomatosis tumor predisposition and is located in a region that is deleted in the great majority (89%) of patients with 22q11.2 deletion syndrome (22q11.2DS). Since it is known that approximately 1 in 500 people in the general population will dev...

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Detalles Bibliográficos
Autores principales: Evans, D. Gareth, Messiaen, Ludwine M., Foulkes, William D., Irving, Rachel E. A., Murray, Alexandra J., Perez-Becerril, Cristina, Rivera, Barbara, McDonald-McGinn, Donna M., Stevenson, David A., Smith, Miriam J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460436/
https://www.ncbi.nlm.nih.gov/pubmed/33879870
http://dx.doi.org/10.1038/s41436-021-01175-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460436/
https://www.ncbi.nlm.nih.gov/pubmed/33879870
http://dx.doi.org/10.1038/s41436-021-01175-0

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