INVESTIGADORES
RIVOLTA Carina Marcela
artículos
Título:
A new compound heterozygous for c.886C>T/c.2206C>T [p.R277X/p.Q717X] mutations in the thyroglobulin gene as a cause of foetal goitrous hypothyroidism.
Autor/es:
CITTERIO, CINTIA E; COUTANT , R; ROULEAU, S; MIRALLES GARCÍA, JM; GONZALEZ-SARMIENTO, ROGELIO; RIVOLTA, CARINA M.; TARGOVNIK, HÉCTOR M.
Revista:
CLINICAL ENDOCRINOLOGY
Editorial:
WILEY-BLACKWELL PUBLISHING, INC
Referencias:
Lugar: Oxford; Año: 2011 vol. 74 p. 533 - 533
ISSN:
0300-0664
Resumen:
A new compound heterozygous for c.886C>T/c.2206C>T [p.R277X/p.Q717X] mutations in the thyroglobulin gene as a cause of foetal goitrous hypothyroidism.