Patients with mutations in Cyclin M2 (CNNM2) suffer from hypomagnesaemia, seizures, and
intellectual disability. Although the molecular function of CNNM2 is under debate, the protein …

Patients with mutations in Cyclin M2 (CNNM2) suffer from hypomagnesaemia, seizures, and
intellectual disability. Although the molecular function of CNNM2 is under debate, the protein …

Methods Generation of CNNM2 deficient mice. Cnnm2−/− mice were generated by
CRISPR/Cas9 mediated genomic editing in murine zygotes 20. In brief, guide RNAs were …

Methods Generation of CNNM2 deficient mice. Cnnm2−/− mice were generated by
CRISPR/Cas9 mediated genomic editing in murine zygotes 20. In brief, guide RNAs were …

Patients with mutations in Cyclin M2 (CNNM2) suffer from hypomagnesaemia, seizures, and
intellectual disability. Although the molecular function of CNNM2 is under debate, the protein …

Patients with mutations in Cyclin M2 (CNNM2) suffer from hypomagnesaemia, seizures, and
intellectual disability. Although the molecular function of CNNM2 is under debate, the protein …

Methods Generation of CNNM2 deficient mice. Cnnm2−/− mice were generated by
CRISPR/Cas9 mediated genomic editing in murine zygotes 20. In brief, guide RNAs were …

Patients with mutations in Cyclin M2 (CNNM2) suffer from hypomagnesaemia, seizures, and
intellectual disability. Although the molecular function of CNNM2 is under debate, the protein …

Patients with mutations in Cyclin M2 (CNNM2) suffer from hypomagnesaemia, seizures, and
intellectual disability. Although the molecular function of CNNM2 is under debate, the protein …

抄録< jats: title> Abstract</jats: title>< jats: p> Patients with mutations in Cyclin M2 (CNNM2)
suffer from hypomagnesaemia, seizures, and intellectual disability. Although the molecular …