Associated Papers
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 1861.653
Gene structure, chromosomal localization, and mutation screening of the human gene for the inner ear protein otospiralin.
Lavigne-Rebillard M et al.
Neurogenetics, 2003
Select a paper to view details