RAB39B Deficiency Impairs Learning and Memory Partially Through Compromising Autophagy
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DOI: 10.3389/fcell.2020.598622
Abstract: RAB39B is located on the X chromosome and encodes the RAB39B protein that belongs to the RAB family. Mutations in RAB39B are known to be associated with X-linked intellectual disability (XLID), Parkinson’s disease, and autism.… read more here.
Keywords: deficiency impairs; rab39b deficiency; rab39b; learning memory ... See more keywords