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Med12
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MED12 variants associated with X-linked recessive partial epilepsy without intellectual disability.
Extensive blaschkoid hypopigmentation in a girl with MED12-related disorder.
Differential Expression of MED12-Associated Coding RNA Transcripts in Uterine Leiomyomas.
Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy.
RISING STARS: Role of MED12 mutation in the pathogenesis of uterine fibroids.
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A Study of Toca 511, a Retroviral Replicating Vector, Combined With Toca FC in Patients With Solid T…
Analysis of Androgene Receptors Axis and DNA Damage Repair Genes in Patients With Prostate Cancer
Study to Evaluate ctDNA of mCSPC Patients Receiving Apalutamide in Japan
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