Matches in Nanopublications for { ?s ?p "[Homozygous or compound heterozygous mutations in SLC19A3 cause two distinct clinical phenotypes, biotin-responsive basal ganglia disease and Wernicke's-like encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP723137.RACw0MZ_4JKgkAS2tBHXXt0lhC3QpX1bu1TCBQjnMPAgQ130_assertion description "[Homozygous or compound heterozygous mutations in SLC19A3 cause two distinct clinical phenotypes, biotin-responsive basal ganglia disease and Wernicke's-like encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723137.RACw0MZ_4JKgkAS2tBHXXt0lhC3QpX1bu1TCBQjnMPAgQ130_provenance.