hmre11造句

• It is a 754 amino acid protein identified as a member of the NBS1 / hMre11 / RAD50 ( N / M / R, more commonly referred to as double strand DNA break repair complex.
• Ataxia-telangiectasia like disorder ( ATLD ) is an extremely rare condition, caused by mutation in the hMre11 gene, that could be considered in the differential diagnosis of A-T . Patients with ATLD are very similar to those with A-T in showing a progressive cerebellar ataxia, hypersensitivity to ionizing radiation and genomic instability.