Associated Papers
Biallelic ZNF407 mutations in a neurodevelopmental disorder with ID, short stature and variable microcephaly, hypotonia, ocular anomalies and facial dysmorphism.
Zahra Q et al.
Journal of Human Genetics, 2020
Mutations in zinc finger 407 [ZNF407] cause a unique autosomal recessive cognitive impairment syndrome.
Kambouris M et al.
Orphanet Journal of Rare Diseases, 2014
Balanced translocation t(3;18)(p13;q22.3) and points mutation in the ZNF407 gene detected in patients with both moderate non-syndromic intellectual disability and autism.
Ren CM et al.
Biochimica Et Biophysica Acta, 2013
Select a paper to view details