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- [3] GM2 Gangliosidosis: Whole-Exome Sequencing Reveals Novel Homozygous Pathogenic Variant within the HEXA Gene in Iranian Family [J]. Russian Journal of Genetics, 2024, 60 : 109 - 120
- [5] Whole-exome sequencing identified a novel variant in an Iranian patient affected by pycnodysostosis [J]. MOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 8 (03):
- [6] Pathogenic mutations in two families with congenital cataract identified with whole-exome sequencing [J]. MOLECULAR VISION, 2013, 19 : 384 - 389
- [8] Whole-exome sequencing identified a novel homozygous ASPH frameshift variant causing Traboulsi syndrome in a Chinese family [J]. MOLECULAR GENETICS & GENOMIC MEDICINE, 2021, 9 (01):
- [10] Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencing [J]. European Journal of Medical Research, 27