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Q36273551-42D37798-AB82-4680-A468-0296DCE1462D
Q36273551-42D37798-AB82-4680-A468-0296DCE1462D
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Statement
http://www.wikidata.org/entity/statement/Q36273551-42D37798-AB82-4680-A468-0296DCE1462D
Point mutations in KAL1 and the mitochondrial gene MT-tRNA(cys) synergize to produce Kallmann syndrome phenotype.
P2860
Q36273551-42D37798-AB82-4680-A468-0296DCE1462D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36273551-42D37798-AB82-4680-A468-0296DCE1462D
rank
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type
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Statement
wasDerivedFrom
2cfcecfaae8206aaf4842426fdbde64bcc78c581
P2860
Kallmann syndrome caused by mutations in the PROK2 and PROKR2 genes: pathophysiology and genotype-phenotype correlations.