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Q34752030-31AE4596-9910-44D3-84D6-9EF3C421F0E3
Q34752030-31AE4596-9910-44D3-84D6-9EF3C421F0E3
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http://www.wikidata.org/entity/statement/Q34752030-31AE4596-9910-44D3-84D6-9EF3C421F0E3
Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency.
P2860
Q34752030-31AE4596-9910-44D3-84D6-9EF3C421F0E3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34752030-31AE4596-9910-44D3-84D6-9EF3C421F0E3
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wasDerivedFrom
5657c9c46b9b4fe1534110fda2f0e861a9f400c8
P2860
Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness