Matches in Nanopublications for { ?s ?p "[Taken together, this report further suggests that hereditary 5-oxoprolinase deficiency is a benign biochemical condition caused by mutations in the OPLAH gene, which are transmitted in an autosomal recessive manner, but 5-oxoprolinuria may be a chance association in other disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_assertion description "[Taken together, this report further suggests that hereditary 5-oxoprolinase deficiency is a benign biochemical condition caused by mutations in the OPLAH gene, which are transmitted in an autosomal recessive manner, but 5-oxoprolinuria may be a chance association in other disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_provenance.
- NP1211304.RABMdT9HO2EWPryV6Cu25uCvjxERajK7tpyolvdbAFGis130_assertion description "[Taken together, this report further suggests that hereditary 5-oxoprolinase deficiency is a benign biochemical condition caused by mutations in the OPLAH gene, which are transmitted in an autosomal recessive manner, but 5-oxoprolinuria may be a chance association in other disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211304.RABMdT9HO2EWPryV6Cu25uCvjxERajK7tpyolvdbAFGis130_provenance.