Clinical exome sequencing (CES) identifies a novel homozygous variant in NECTIN1 causing CLPED1

Yılmaz Güleç, ElifBudak, Gülden2025-04-172025-04-172024Yılmaz Güleç, E., & Budak, G. (2024). Clinical exome sequencing (CES) identifies a novel homozygous variant in NECTIN1 causing CLPED1. European Journal of Human Genetics, 32, pp. 999-1000. Berlin, Germany1018-4813https://hdl.handle.net/20.500.13055/948Clinical exome sequencing (CES) identifies a novel homozygous variant in NECTIN1 causing CLPED1eninfo:eu-repo/semantics/openAccessClinical exome sequencing (CES) identifies a novel homozygous variant in NECTIN1 causing CLPED1Conference Object329991000Q2WOS:001407868900280