Macken WL et al. Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly. Genome Med. 2021; 13(1):34. PMID: 33632302.
COPB1
Macken WL et al. Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly. Genome Med. 2021; 13(1):34. PMID: 33632302.