Varaico: Literature-Extracted Genetic Variants

Gene:MYRF
Variant:p.F387L
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MYRF

NM_001127392.3:p.F387L

Associated Papers

Signaling pathway screening platforms are an efficient approach to identify therapeutic targets in cancers that lack known driver mutations: a case report for a cancer of unknown primary origin.

Torres-Ayuso P et al.

Npj Genomic Medicine, 2018

29951225 (PubMed )
Supplement: 41525_2018_55_MOESM2_ESM.xls › Sup_File_1

Functional mechanisms of MYRF DNA-binding domain mutations implicated in birth defects.

Fan C et al.

The Journal of Biological Chemistry, 0

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