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A novel variant of C12orf4 in a consanguineous Armenian family confirms the etiology of autosomal recessive intellectual disability type 66 with delineation of the phenotype

Author / Creator:Hancarova, Miroslava ; Babikyan, Davit ; Bendova, Sarka ; Midyan, Susanna ; Prchalova, Darina ; Shahsuvaryan, Gohar ; Stranecky, Viktor ; Sarkisian, Tamara ; Sedlacek, Zdenek

Publisher:United States: John Wiley & Sons, Inc

Journal title:Molecular genetics & genomic medicine, 2019-09, Vol.7 (9), p.e865-n/a

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A novel variant of C12orf4 in a consanguineous Armenian family confirms the etiology of autosomal recessive intellectual disability type 66 with delineation of the phenotype

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