Matches in Nanopublications for { ?s ?p "[Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP135478.RACiqAw324tkOhMeZew2c2HvcbSb1K6-crc6eij5DXpio130_assertion description "[Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135478.RACiqAw324tkOhMeZew2c2HvcbSb1K6-crc6eij5DXpio130_provenance.
- NP6719.RAzVk9OW0_a0NYD0lbTlQe5RZypxTbzYas0VfOB4xi9iE130_assertion description "[Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6719.RAzVk9OW0_a0NYD0lbTlQe5RZypxTbzYas0VfOB4xi9iE130_provenance.
- assertion description "[Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_assertion description "[Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_provenance.
- NP1208.RAA96qJgzrJUY12kxiUjyHnQ3_LOeLXNhHU0rUd3HgYOA130_assertion description "[Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1208.RAA96qJgzrJUY12kxiUjyHnQ3_LOeLXNhHU0rUd3HgYOA130_provenance.
- NP193758.RAlYgIOp_GMnHnPeNFE1HIkZUzAYO6Suoz7Rle-UyBFKo130_assertion description "[Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193758.RAlYgIOp_GMnHnPeNFE1HIkZUzAYO6Suoz7Rle-UyBFKo130_provenance.
- NP1948.RAz6MTLmBfeoeV2aoEwY1WUbcm8lTchniyCgdgrm0D6Qs130_assertion description "[Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1948.RAz6MTLmBfeoeV2aoEwY1WUbcm8lTchniyCgdgrm0D6Qs130_provenance.