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Summary Anatomy Item Literature (7748) Expression Attributions Wiki
XB-ANAT-11

Papers associated with brain (and l1cam)

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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.    

Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus., Date P., Sci Rep. April 17, 2019; 9 (1): 6196.                            

Role of the visual experience-dependent nascent proteome in neuronal plasticity., Liu HH., Elife. February 7, 2018; 7                     

Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome., Karpinski BA., Dis Model Mech. February 1, 2014; 7 (2): 245-57.                

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