FOXD4 c.442T>A ;(p.W148R)
Variant ID: 9-117678-A-T
NM_207305.4(FOXD4):c.442T>A;(p.W148R)
This variant was identified in 2 publications
Variant-Specific Resource Links:
Publications:
Insights into the Cardiac Phenotype in 9p Deletion Syndrome: A Multicenter Italian Experience and Literature Review.
Genes
Pugnaloni, Flaminia F; Onesimo, Roberta R; Blandino, Rita R; Putotto, Carolina C; Versacci, Paolo P; Delogu, Angelica Bibiana AB; Leoni, Chiara C; Trevisan, Valentina V; Croci, Ileana I; Calì, Federica F; Digilio, Maria Cristina MC; Zampino, Giuseppe G; Marino, Bruno B; Calcagni, Giulio G
Publication Date: 2023-01-05
Variant appearance in text: FOXD4: W148R
Variant Present in the following documents:
Massive Loss of Transcription Factors Promotes the Initial Diversification of Placental Mammals.
International Journal Of Molecular Sciences
Zhao, Xin-Wei XW; Wu, Jiaqi J; Kishino, Hirohisa H; Chen, Ling L
Publication Date: 2022-08-26
Variant appearance in text: FOXD4: W148R
Variant Present in the following documents: