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<i>KIF21A</i>-associated peripheral neuropathy defined by impaired binding with TUBB3.
Not available
S-EPMC11773626
|
biostudies-literature
Cite
Genome sequencing reveals novel noncoding variants in PLA2G6 and LMNB1 causing progressive neurologic disease.
Not available
S-EPMC9000935
|
biostudies-literature
Cite
Advancing Equity in Rare Disease Research: Insights From the Undiagnosed Disease Network.
Not available
S-EPMC11698638
|
biostudies-literature
Cite
Missense variants in <i>TUBA4A</i> cause myo-tubulinopathies.
Not available
S-EPMC12262762
|
biostudies-literature
Cite
Genome Sequencing for Diagnosing Rare Diseases.
Not available
S-EPMC11350637
|
biostudies-literature
Cite
Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling.
Not available
S-EPMC6925349
|
biostudies-literature
Cite
Changes in symptomatology, reinfection, and transmissibility associated with the SARS-CoV-2 variant B.1.1.7: an ecological study.
Not available
S-EPMC8041365
|
biostudies-literature
Cite
COVID-19 due to the B.1.617.2 (Delta) variant compared to B.1.1.7 (Alpha) variant of SARS-CoV-2: a prospective observational cohort study.
Not available
S-EPMC9240087
|
biostudies-literature
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Genomic assessment of quarantine measures to prevent SARS-CoV-2 importation and transmission.
Not available
S-EPMC8866425
|
biostudies-literature
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SARS-CoV-2 Omicron is an immune escape variant with an altered cell entry pathway.
Not available
S-EPMC9352574
|
biostudies-literature
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