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UnknownWhole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems.
Not available
S-EPMC7325133 | biostudies-literature
UnknownInvestigation of genetic causes of intellectual disability in kerman province, South East of iran.
Not available
S-EPMC3372047 | biostudies-literature
UnknownThe Use of Hexokinase 2-Displacing Peptides as an Anti-Neoplastic Approach for Malignant Peripheral Nerve Sheath Tumors.
Not available
S-EPMC11240344 | biostudies-literature
UnknownBi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia.
Not available
S-EPMC7413886 | biostudies-literature
UnknownBiallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
Not available
S-EPMC8219359 | biostudies-literature
UnknownBurden of 375 diseases and injuries, risk-attributable burden of 88 risk factors, and healthy life expectancy in 204 countries and territories, including 660 subnational locations, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023.
Not available
S-EPMC12535840 | biostudies-literature
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