Top Tweets for #PRDM5
#BCS affects 1/1,000,000 people. Caused by changes in #PRDM5 or #ZNF469 genes, it is a recessive condition. Both copies of the gene inherited from parents by affected individuals carry faulty genetic instructions (DNA) so PRDM5 or ZNF469 do not work correctly. #RareDiseaseDay *CS
Today’s #GeneOfTheDay is #Prdm5. Full name: PR domain containing 5; Human disease models: Brittle Cornea Syndrome. Mouse knockout phenotype associations include increased/ absent threshold for auditory brainstem response & abnormal optic disc morphology. https://t.co/2QL5bbgVe2
Today’s #GeneOfTheDay is #Prdm5. Full name: PR domain containing 5; Knockout phenotype associations include increased/ absent threshold for auditory brainstem response & abnormal optic disc morphology. Human disease models: Brittle Cornea Syndrome https://t.co/ZBoJ9d8WC4
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