'''RasGEF domain family, member 1A''' is a [[protein]] that in humans is encoded by the RASGEF1A [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: RasGEF domain family, member 1A | url = https://www.ncbi.nlm.nih.gov/gene/221002 }}</ref>
'''RasGEF domain family, member 1A''' is a [[protein]] that in humans is encoded by the RASGEF1A [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: RasGEF domain family, member 1A | url = https://www.ncbi.nlm.nih.gov/gene/221002 }}</ref>
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Emison ES, McCallion AS, Kashuk CS, Bush RT, Grice E, Lin S, Portnoy ME, Cutler DJ, Green ED, Chakravarti A (Apr 2005). "A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk". Nature. 434 (7035): 857–63. doi:10.1038/nature03467. PMID15829955.
Yaman E, Gasper R, Koerner C, Wittinghofer A, Tazebay UH (Aug 2009). "RasGEF1A and RasGEF1B are guanine nucleotide exchange factors that discriminate between Rap GTP-binding proteins and mediate Rap2-specific nucleotide exchange". The FEBS Journal. 276 (16): 4607–16. doi:10.1111/j.1742-4658.2009.07166.x. PMID19645719.
