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XB-ANAT-3637
Papers associated with striatum (and hhip)
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SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus., Jin SC., Mol Genet Genomic Med. September 1, 2019; 7 (9): e892. |
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Mutations underlying Episodic Ataxia type-1 antagonize Kv1.1 RNA editing., Ferrick-Kiddie EA., Sci Rep. February 20, 2017; 7 41095. |
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