Matches in Nanopublications for { ?s ?p "[Classic Bartter syndrome is due to a mutation in the gene encoding the chloride channel (CLCNKB), also a regulator of NKCC2, and typically presents in infancy or early childhood with failure to thrive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_assertion description "[Classic Bartter syndrome is due to a mutation in the gene encoding the chloride channel (CLCNKB), also a regulator of NKCC2, and typically presents in infancy or early childhood with failure to thrive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_provenance.
- assertion description "[Classic Bartter syndrome is due to a mutation in the gene encoding the chloride channel (CLCNKB), also a regulator of NKCC2, and typically presents in infancy or early childhood with failure to thrive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.