المؤلفون: Qian Zhang, Shuya Yang, Xin Chen, Hongdan Wang, Keyan Li, Chaonan Zhang, Shixiu Liao, Litao Qin, Qiaofang Hou

المصدر: Frontiers in Genetics, Vol 14 (2023)

مصطلحات موضوعية: Meckel Syndrome, TMEM231 gene, whole exome sequencing, splicing mutation, alternative transcription, primary cilia, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2023.1252873/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/63832186ae2e43a78d25656518c27fda

المؤلفون: Qian Zhang, Shuya Yang, Xin Chen, Hongdan Wang, Keyan Li, Chaonan Zhang, Shixiu Liao, Litao Qin, Qiaofang Hou

مصطلحات موضوعية: Genetics, Genetic Engineering, Biomarkers, Developmental Genetics (incl. Sex Determination), Epigenetics (incl. Genome Methylation and Epigenomics), Gene Expression (incl. Microarray and other genome-wide approaches), Genome Structure and Regulation, Genomics, Genetically Modified Animals, Livestock Cloning, Gene and Molecular Therapy, Meckel Syndrome, TMEM231 gene, whole exome sequencing, splicing mutation, alternative transcription, primary cilia

Relation: https://figshare.com/articles/dataset/Table1_Identification_of_novel_TMEM231_gene_splice_variants_and_pathological_findings_in_a_fetus_with_Meckel_Syndrome_xlsx/24086211

الاتاحة: https://doi.org/10.3389/fgene.2023.1252873.s005
https://figshare.com/articles/dataset/Table1_Identification_of_novel_TMEM231_gene_splice_variants_and_pathological_findings_in_a_fetus_with_Meckel_Syndrome_xlsx/24086211