Presence of the G1138A mutation in the FGFR3 coding gene in a group of Cuban achondroplasia patients

Article

Abstract: Achondroplasia, inherited as an autosomal dominant trait, is the most common human skeletal dysplasi

Palabras claves:

Achondroplasia, Autosomal dominant, FGFR3, Hipoachondroplasia, Osteochondrodysplasias, Thanatophoric dysplasia

Autores:

Avella A.B., Baute L.H., Fernandez S.O., Mesa T.C., Peralta E.M., Thelvia I. Ramos Gómez

Fuentes:

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scopus