Associated Papers
Uncovering common genetic risk factors in migraine and epilepsy through whole exome sequencing.
Sahu P et al.
Epileptic Disorders : International Epilepsy Journal With Videotape, 2025
Assessment of 1863 GRIN2A Variants Contradicts a Role in Tumorigenesis.
Jauss RT et al.
International Journal of Molecular Sciences, 2025
40565021 (PubMed )
Supplement: ijms-26-05558-s001.zip › Supplementary_Table_S1.xlsx › Sheet_1
Somatic mutation of GRIN2A in malignant melanoma results in loss of tumor suppressor activity via aberrant NMDAR complex formation.
Prickett TD et al.
The Journal of Investigative Dermatology, 2014
24739903 (PubMed )
Supplement: NIHMS585518-supplement-supplement_1.pdf
Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
Wei X et al.
Nature Genetics, 2011
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