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Volume 60, Issue 9
Pathogenic variations in MAML2 and MAMLD1 contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway
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Genotype-phenotype correlations
Original research
Pathogenic variations in
MAML2
and
MAMLD1
contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway
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