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UnknownMRI Patterns Distinguish AQP4 Antibody Positive Neuromyelitis Optica Spectrum Disorder From Multiple Sclerosis.
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S-EPMC8458658 | biostudies-literature
UnknownNormal and pathogenic variation of RFC1 repeat expansions: implications for clinical diagnosis.
Not available
S-EPMC10689911 | biostudies-literature
UnknownAn ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.
Not available
S-EPMC8263055 | biostudies-literature
UnknownAVERT2 (a very early rehabilitation trial, a very effective reproductive trigger): retrospective observational analysis of the number of babies born to trial staff.
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S-EPMC4676118 | biostudies-literature
UnknownAccelarated immune ageing is associated with COVID-19 disease severity.
Not available
S-EPMC10782727 | biostudies-literature
UnknownSpectrum of mutational signatures in T-cell lymphoma reveals a key role for UV radiation in cutaneous T-cell lymphoma.
Not available
S-EPMC7889847 | biostudies-literature
UnknownHeterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy.
Not available
S-EPMC7862057 | biostudies-literature
UnknownGWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements.
Not available
S-EPMC9385867 | biostudies-literature
UnknownUsing data from the 100,000 Genomes Project to resolve conflicting interpretations of a recurrent <i>TUBB2A</i> mutation.
Not available
S-EPMC8961759 | biostudies-literature
UnknownA systematic CRISPR screen defines mutational mechanisms underpinning signatures caused by replication errors and endogenous DNA damage.
Not available
S-EPMC7611045 | biostudies-literature
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