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Clinical Features and Genetic Variants in Chinese Children With Pyridoxine-Dependent Epilepsy
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2025-08-18
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File including all data used in the article
PROG = line ID SPECIES = common species name ID = sample ID DATE = day of capture (day 1 = January 1) AGE = age of individual (0 = second year; 1 = older) SEX = sex of the individual (1 = male; 2 = fe
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Supplementary Material for: Fahr's Disease Linked to a Novel SLC20A2 Gene Mutation Manifesting with Dynamic Aphasia
Background: Idiopathic basal ganglia calcification (IBGC), also known as Fahr's disease, is a rare disorder characterized by widespread cerebral calcifications, an autosomal dominant pattern of inheri
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Neurospora crassa strain:FGSC 11999 Genome sequencing. Neurospora crassa strain:FGSC 11999
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Genotyping frequencies and the association of genotype with disease progression during ADT.
Abbreviations: ADT, androgen-deprivation therapy; HR, hazard ratio; 95% CI, 95% confidence interval; PSA, prostate-specific antigen. *P values were calculated using the log-rank test. †HRs were adjust
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Neurospora crassa strain:FGSC 3641 Genome sequencing. Neurospora crassa strain:FGSC 3641
Connecting fungal phenotypes to genotypes in Neurospora crassa
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