Associated Papers
Spondyloocular Syndrome: A Report of an Additional Family and Phenotypic Spectrum Delineation.
Chouery E et al.
Genes, 2023
36833424 (PubMed )
Supplement: genes-14-00497-s001.zip › genes-2215459-supplementary.xlsx › Sheet1
Single-cell sequencing reveals CD133+CD44--originating evolution and novel stemness related variants in human colorectal cancer.
Zhang X et al.
Ebiomedicine, 2022
35785618 (PubMed )
Supplement: mmc1.xlsx › Supplementary_Table_2b
Spondyloocular Syndrome: A Novel XYLT2 Variant with Description of the Neonatal Phenotype.
Doddato G et al.
Frontiers in Genetics, 2021
Intrafamilial variability of XYLT2-related spondyloocular syndrome.
Guleray N et al.
European Journal of Medical Genetics, 2019
A Novel Homozygous Frameshift Variant in XYLT2 Causes Spondyloocular Syndrome in a Consanguineous Pakistani Family.
Kausar M et al.
Frontiers in Genetics, 2019
Homozygous XYLT2 variants as a cause of spondyloocular syndrome.
Umair M et al.
Clinical Genetics, 2018
Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects.
Munns CF et al.
American Journal of Human Genetics, 2015
An association between bilateral keratoconus in a patient with spondyloocular syndrome and xylosyltransferase II gene mutation.
Fathi-Nieto S et al.
Oman Journal of Ophthalmology, 0
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