Exome sequencing revealed a novel homozygous variant in TRMT61 A in a multiplex family with atypical Cornelia de Lange Syndrome from Rwanda.
外显子组测序揭示了来自卢旺达的一个患有非典型 Cornelia de Lange 综合征的多重家族中 TRMT61 A 的一个新的纯合变异
期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-025-02153-0
Uwibambe Esther, Yalcouyé Abdoulaye, Aboagye Elvis Twumasi, Xhakaza Lettilia, Popel Kalinka, Dukuze Norbert, Bharadwaj Thashi, de Kock Carmen, Schrauwen Isabelle, Leal Suzanne M, Mutesa Leon, Wonkam Ambroise