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- NP278617.RAH4cNAn-qmHb_IlFeV5LbiPpuYdfoCmkQao3KhcUXPxA130_assertion type Assertion NP278617.RAH4cNAn-qmHb_IlFeV5LbiPpuYdfoCmkQao3KhcUXPxA130_head.
- NP278617.RAH4cNAn-qmHb_IlFeV5LbiPpuYdfoCmkQao3KhcUXPxA130_assertion wasGeneratedBy ECO_0000203 NP278617.RAH4cNAn-qmHb_IlFeV5LbiPpuYdfoCmkQao3KhcUXPxA130_provenance.
- NP278617.RAH4cNAn-qmHb_IlFeV5LbiPpuYdfoCmkQao3KhcUXPxA130_assertion wasDerivedFrom befree-2016 NP278617.RAH4cNAn-qmHb_IlFeV5LbiPpuYdfoCmkQao3KhcUXPxA130_provenance.
- NP278617.RAH4cNAn-qmHb_IlFeV5LbiPpuYdfoCmkQao3KhcUXPxA130_assertion SIO_000772 10727999 NP278617.RAH4cNAn-qmHb_IlFeV5LbiPpuYdfoCmkQao3KhcUXPxA130_provenance.
- NP278617.RAH4cNAn-qmHb_IlFeV5LbiPpuYdfoCmkQao3KhcUXPxA130_assertion evidence source_evidence_literature NP278617.RAH4cNAn-qmHb_IlFeV5LbiPpuYdfoCmkQao3KhcUXPxA130_provenance.
- NP278617.RAH4cNAn-qmHb_IlFeV5LbiPpuYdfoCmkQao3KhcUXPxA130_assertion description "[Mutations in the KAL gene (Kallmann syndrome) and the AHC gene (adrenal hypoplasia congenita/HH) cause X-linked recessive HH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278617.RAH4cNAn-qmHb_IlFeV5LbiPpuYdfoCmkQao3KhcUXPxA130_provenance.