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Published in 2020 at "Nucleic Acids Research"
DOI: 10.1093/nar/gkaa636
Abstract: Abstract Microcephalin 1 (MCPH1) was identified from genetic mutations in patients with primary autosomal recessive microcephaly. In response to DNA double-strand breaks (DSBs), MCPH1 forms damage-induced foci and recruits BRCA2–RAD51 complex, a key component of…
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Keywords:
protein;
microcephaly family;
family protein;
protein mcph1 ... See more keywords