Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases.
Miller DE, Lee L, Galey M, Kandhaya-Pillai R, Tischkowitz M, Amalnath D, Vithlani A, Yokote K, Kato H, Maezawa Y, Takada-Watanabe A, Takemoto M, Martin GM, Eichler EE, Hisama FM, Oshima J.
Miller DE, et al. Among authors: kandhaya pillai r.
J Med Genet. 2022 May 9;59(11):1087-94. doi: 10.1136/jmedgenet-2022-108485. Online ahead of print.
J Med Genet. 2022.
PMID: 35534204
Free PMC article.