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THRB gene mutation
Clinical significance:
- defects in THRB are the cause of:
a) generalized thyroid hormone resistance
b) selective pituitary thyroid hormone resistance
Related
thyroid hormone receptor beta; nuclear receptor subfamily 1 group A member 2 (THRB, ERBA2, NR1A2, THR1)
General
gene mutation testing; gene mutation analysis
References
Loinc