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 › 1907.666
Fine mapping of new glaucoma locus GLC1M and exclusion of neuregulin 2 as the causative gene.
Fan BJ et al.
Molecular Vision, 2007
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