Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases

BACKGROUND: Werner syndrome (WS) is an autosomal recessive progeroid syndrome caused by variants in WRN. The International Registry of Werner Syndrome has identified biallelic pathogenic variants in 179/188 cases of classical WS. In the remaining nine cases, only one heterozygous pathogenic variant...

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Detalles Bibliográficos
Autores principales: Miller, Danny E., Lee, Lin, Galey, Miranda, Kandhaya-Pillai, Renuka, Tischkowitz, Marc, Amalnath, Deepak, Vithlani, Avadh, Yokote, Koutaro, Kato, Hisaya, Maezawa, Yoshiro, Takada-Watanabe, Aki, Takemoto, Minoru, Martin, George M., Eichler, Evan E., Hisama, Fuki M., Oshima, Junko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Diagnostics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613861/
https://www.ncbi.nlm.nih.gov/pubmed/35534204
http://dx.doi.org/10.1136/jmedgenet-2022-108485

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613861/
https://www.ncbi.nlm.nih.gov/pubmed/35534204
http://dx.doi.org/10.1136/jmedgenet-2022-108485

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