The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2)

GAC Franken, D Müller, C Mignot, B Keren… - Human …, 2021 - Wiley Online Library
Hypomagnesemia, seizures, and intellectual disability (HSMR) syndrome is a rare disorder
caused by mutations in the cyclin M2 (CNNM2) gene. Due to the limited number of cases …
被引用次数：23 相关文章

The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2)

GAC Franken, D Müller, C Mignot, B Keren… - Human …, 2021 - pubmed.ncbi.nlm.nih.gov
Hypomagnesemia, seizures, and intellectual disability (HSMR) syndrome is a rare disorder
caused by mutations in the cyclin M2 (CNNM2) gene. Due to the limited number of cases …

The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2).

GAC Franken, D Müller, C Mignot, B Keren, J Lévy… - Human …, 2021 - europepmc.org
Hypomagnesemia, seizures, and intellectual disability (HSMR) syndrome is a rare disorder
caused by mutations in the cyclin M2 (CNNM2) gene. Due to the limited number of cases …

The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2)

GAC Franken, D Müller, C Mignot, B Keren… - Human …, 2021 - repozitorij.mef.unizg.hr
Hypomagnesemia, seizures, and intellectual disability (HSMR) syndrome is a rare disorder
caused by mutations in the cyclin M2 (CNNM2) gene. Due to the limited number of cases …

The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2)

GAC Franken, D Muller, C Mignot, B Keren… - Human …, 2021 - hal.sorbonne-universite.fr
Hypomagnesemia, seizures, and intellectual disability (HSMR) syndrome is a rare disorder
caused by mutations in the cyclin M2 (CNNM2) gene. Due to the limited number of cases …
[PDF] ru.nl

[PDF][PDF] The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2).

GAC Franken, D Müller, C Mignot, B Keren, J Lévy… - 2021 - repository.ubn.ru.nl
Hypomagnesemia, seizures, and intellectual disability (HSMR) syndrome is a rare disorder
caused by mutations in the cyclin M2 (CNNM2) gene. Due to the limited number of cases …

The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2)

GAC Franken, D Muller, C Mignot, B Keren, J Levy… - Human Mutation, 2021 - hal.science
Hypomagnesemia, seizures, and intellectual disability (HSMR) syndrome is a rare disorder
caused by mutations in the cyclin M2 (CNNM2) gene. Due to the limited number of cases …

The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2)

GAC Franken, D Müller, C Mignot, B Keren… - Human …, 2021 - repozitorij.unizg.hr
Hypomagnesemia, seizures, and intellectual disability (HSMR) syndrome is a rare disorder
caused by mutations in the cyclin M2 (CNNM2) gene. Due to the limited number of cases …
[HTML] nih.gov

[HTML][HTML] The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2)

GAC Franken, D Müller, C Mignot, B Keren… - Human …, 2021 - ncbi.nlm.nih.gov
Hypomagnesemia, seizures, and intellectual disability (HSMR) syndrome is a rare disorder
caused by mutations in the cyclin M2 (CNNM2) gene. Due to the limited number of cases …

The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2)

GAC Franken, D Müller, C Mignot, B Keren… - Human …, 2021 - repozitorij.mef.unizg.hr
Abstract (english) Hypomagnesemia, seizures, and intellectual disability (HSMR) syndrome
is a rare disorder caused by mutations in the cyclin M2 (CNNM2) gene. Due to the limited …