Author: Alkhater, Reem A.; Wang, Peixiang; Ruggieri, Alessandra; Israelian, Lori; Walker, Susan; Scherer, Stephen W.; Smith, Mary Lou; Minassian, Berge A.
Title: Dominant LMAN2L mutation causes intellectual disability with remitting epilepsy Document date: 2019_3_7
ID: 5rt5vuwu_23
Snippet: Additional supporting information may be found online in the Supporting Information section at the end of the article. Table S1 . Current neuropsychological testing data. Table S2 . Summary of shared heterozygous, protein coding variants with high confidence in the linked region amongst affected patients......
Document: Additional supporting information may be found online in the Supporting Information section at the end of the article. Table S1 . Current neuropsychological testing data. Table S2 . Summary of shared heterozygous, protein coding variants with high confidence in the linked region amongst affected patients.
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