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Literature summary for 2.7.10.1 extracted from

  • Meyers, G.A.; Day, D.; Goldberg, R.; Daentl, D.L.; Przylepa, K.A.; Abrams, L.J.; Graham, J.M., Jr.; Feingold, M.; Moeschler, J.B.; Rawnsley, E.; Scott, A.F.; Jabs, E.W.
    FGFR2 Exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicing (1996), Am. J. Hum. Genet., 58, 491-498.
    View publication on PubMedView publication on EuropePMC
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Protein Variants

Protein Variants Comment Organism
additional information FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes, missense changes, insertions, and a deletion due to alternative RNA splicing Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens P21802
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-

Synonyms

Synonyms Comment Organism
fibroblast growth factor receptor 2
-
 Homo sapiens