PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 34732557-3 2021 This syndrome is related to an inherited neurodegenerative disorder"s heterogeneous group characterized by the accumulation of iron in the brain, caused by a mutation in the DCAF17 gene. Iron 127-131 DDB1 and CUL4 associated factor 17 Homo sapiens 174-180 33417382-1 2020 PURPOSE: Woodhouse-Sakati syndrome is a rare autosomal recessive syndrome caused by homozygous mutations in the DCAF17 gene, characterized by marked neurologic and endocrine manifestations in the setting of brain iron accumulation and white matter lesions on neuroimaging. Iron 213-217 DDB1 and CUL4 associated factor 17 Homo sapiens 112-118 31152917-0 2019 A case of Woodhouse-Sakati syndrome with pituitary iron deposition, cardiac and intestinal anomalies, with a novel mutation in DCAF17. Iron 51-55 DDB1 and CUL4 associated factor 17 Homo sapiens 127-133 31152917-3 2019 We present a new case with pituitary iron deposition, cardiac and intestinal anomalies, with a novel mutation in DCAF17 gene. Iron 37-41 DDB1 and CUL4 associated factor 17 Homo sapiens 113-119 27240811-2 2016 This syndrome belongs to a heterogeneous group of inherited neurodegenerative disorders characterized iron accumulation in the brain, and it is caused by mutations of the C2orf37 gene. Iron 102-106 DDB1 and CUL4 associated factor 17 Homo sapiens 171-178