Severe congenital hypothyroidia in homozygous mutation of the thyroid stimulating hormone receptor gene the thyroid peroxidase and tyroglobulin genes in Moroccan children
| Autor: | Touzani, A., Deroux, N., Gaouzi, A., Kriouile, Y., Chabraoui, L. |
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| Zdroj: | In Clinica Chimica Acta June 2019 493 Supplement 1:S346-S347 |
| Databáze: | ScienceDirect |
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