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Q47735813-0E0FB19F-CA3B-4741-A44B-F12BE82A7280
Q47735813-0E0FB19F-CA3B-4741-A44B-F12BE82A7280
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47735813-0E0FB19F-CA3B-4741-A44B-F12BE82A7280
A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome.
P2860
Q47735813-0E0FB19F-CA3B-4741-A44B-F12BE82A7280
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47735813-0E0FB19F-CA3B-4741-A44B-F12BE82A7280
rank
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type
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Statement
wasDerivedFrom
52eeb5c99e53a10ec69fa8fb3a56b818722de382
P2860
Complete androgen insensitivity syndrome caused by a novel splice donor site mutation and activation of a cryptic splice donor site in the androgen receptor gene.