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Q34365195-3D2ABE0B-E168-4F43-B9BF-5810CFB65AF9
Q34365195-3D2ABE0B-E168-4F43-B9BF-5810CFB65AF9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34365195-3D2ABE0B-E168-4F43-B9BF-5810CFB65AF9
Defect in MAPK signaling as a cause for monogenic obesity caused by inactivating mutations in the melanocortin-4 receptor gene.
P2860
Q34365195-3D2ABE0B-E168-4F43-B9BF-5810CFB65AF9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34365195-3D2ABE0B-E168-4F43-B9BF-5810CFB65AF9
rank
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type
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wasDerivedFrom
984483961bc963717c4be86aaa1be36649ee8917
P2860
A familial thyrotropin (TSH) receptor mutation provides in vivo evidence that the inositol phosphates/Ca2+ cascade mediates TSH action on thyroid hormone synthesis.