CYP17A1 intron mutation causing cryptic splicing in 17α-hydroxylase deficiency

Article

Abstract: 17α-hydroxylase/17, 20-lyase deficiency (17OHD) is an autosomal recessive disease causing congenital

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Autores:

Chao M.C., Chen H.C., Holterhus P.M., Hung C.C., Hwang D.Y., Hwang S.J., Kulle A.E., Kuo M.C., Richard J. Auchus, Riepe F.G.

Fuentes:

scopus