Identification of a second genetic alteration in patients with SHOX deficiency individuals: a potential explanation for phenotype variability.

Published in:

European Journal of Endocrinology, 2023, v. 189, n. 3, p. 387, doi. 10.1093/ejendo/lvad128

By:

• Dantas, Naiara C. B.;
• Funari, Mariana F. A.;
• Lerário, Antonio M.;
• Andrade, Nathalia L. M.;
• Rezende, Raíssa C.;
• Cellin, Laurana P.;
• Alves, Crésio;
• Crisostomo, Lindiane G.;
• Arnhold, Ivo J. P.;
• Mendonca, Berenice;
• Scalco, Renata C.;
• Jorge, Alexander A. L.

Publication type:

Article