Screening of potential novel candidate genes in schwannomatosis patients

Schwannomatosis comprises a group of hereditary tumor predisposition syndromes characterized by, usually benign, multiple nerve sheath tumors, which frequently cause severe pain that does not typically respond to drug treatments. The most common schwannomatosis‐associated gene is NF2, but SMARCB1 an...

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Detalles Bibliográficos
Autores principales: Perez‐Becerril, Cristina, Wallace, Andrew J., Schlecht, Helene, Bowers, Naomi L., Smith, Philip T., Gokhale, Carolyn, Eaton, Helen, Charlton, Chris, Robinson, Rachel, Charlton, Ruth S., Evans, D. Gareth, Smith, Miriam J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540472/
https://www.ncbi.nlm.nih.gov/pubmed/35723634
http://dx.doi.org/10.1002/humu.24424

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540472/
https://www.ncbi.nlm.nih.gov/pubmed/35723634
http://dx.doi.org/10.1002/humu.24424

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