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XB-ANAT-468
Papers associated with whole organism (and cop1)
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Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly., Macken WL., Genome Med. February 25, 2021; 13 (1): 34. |
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Mammalian tribbles homologs at the crossroads of endoplasmic reticulum stress and Mammalian target of rapamycin pathways., Cunard R., Scientifica (Cairo). January 1, 2013; 2013 750871. |
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