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Q35206200-04953CD2-3240-4F75-AF83-442A3224CE32
Q35206200-04953CD2-3240-4F75-AF83-442A3224CE32
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http://www.wikidata.org/entity/statement/Q35206200-04953CD2-3240-4F75-AF83-442A3224CE32
An intronic SNP in the thyroid hormone receptor β gene is associated with pituitary cell-specific over-expression of a mutant thyroid hormone receptor β2 (R338W) in the index case of pituitary-selective resistance to thyroid hormone.
P2860
Q35206200-04953CD2-3240-4F75-AF83-442A3224CE32
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35206200-04953CD2-3240-4F75-AF83-442A3224CE32
rank
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type
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wasDerivedFrom
c50f39e5f78addba7a7e7f66946eda21b3a2d8a0
P2860
A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.