Pages that link to "Q58236878"
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The following pages link to Maria Lidia Mignogna (Q58236878):
Displaying 6 items.
- Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly (Q24299324) (← links)
- Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology (Q34657526) (← links)
- The intellectual disability protein RAB39B selectively regulates GluA2 trafficking to determine synaptic AMPAR composition. (Q35247088) (← links)
- RAB GTPases and RAB-interacting proteins and their role in the control of cognitive functions. (Q38177517) (← links)
- Critical importance of RAB proteins for synaptic function. (Q39113567) (← links)
- X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene. (Q47887711) (← links)