Varaico: Literature-Extracted Genetic Variants

Gene:NRCAM
Variant:p.H539D
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NRCAM

NM_001037132.4:p.H539D

Associated Papers

Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome).

Javadiyan S et al.

Bmc Medical Genetics, 2017

28482824 (PubMed )
Supplement: 12881_2017_414_MOESM2_ESM.xlsx › Exonic_variants
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."