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Phenotypic Analysis of Patients with SMC1A Mutations and Epilepsy

the Cornelia de Lange Syndrome (CdLS) Foundation USA
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The NIPBL gene codes for a protein which is part of the regulatory centre of cohesin and, along with another gene (MAU2) helps the ring to be loaded onto the duplicated DNA. Changes (mutations) in NIPBL can be found in approximately 70% of individuals with CdLS. 

Classic CdLS is usually caused by changes in NIPBL.

                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                

Trova altre pagine che condividono lo stesso argomento di questa pagina Autonomic nervous system6 Seizures1 SMC1A4 SMC1A1