Mutation creating a new splice site in the growth hormone receptor genes of 37 Ecuadorean patients with Laron syndrome

Article

Abstract: Laron syndrome is an autosomal recessive condition characterized by resistance to growth hormone. We

Palabras claves:

Growth hormone receptor, Laron dwarfism, mutation, RNA splicing

Autores:

Berg M.A., Francke U., Jaime Guevara-Aguirre, Rosenbloom A.L., Rosenfeld R.G.

Fuentes:

scopus