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Severe congenital hypothyroidia in homozygous mutation of the thyroid stimulating hormone receptor gene the thyroid peroxidase and tyroglobulin genes in Moroccan children
Touzani, A., Deroux, N., Gaouzi, A., Kriouile, Y., Chabraoui, L.Volume:
493
Language:
english
Journal:
Clinica Chimica Acta
DOI:
10.1016/j.cca.2019.03.748
Date:
June, 2019
File:
PDF, 104 KB
english, 2019