Matches in Nanopublications for { ?s ?p "[We find that loss of DUOX2 activity results in transient congenital hypothyroidism and that transient congenital hypothyroidism caused by DUOX2 mutations is inherited as an autosomal recessive trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_assertion description "[We find that loss of DUOX2 activity results in transient congenital hypothyroidism and that transient congenital hypothyroidism caused by DUOX2 mutations is inherited as an autosomal recessive trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596646.RA_51hQbvzvQq-Zh9BkOmjxNqwvoVeGxUYdXwHkvtVBdo130_provenance.
- assertion description "[We find that loss of DUOX2 activity results in transient congenital hypothyroidism and that transient congenital hypothyroidism caused by DUOX2 mutations is inherited as an autosomal recessive trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_assertion description "[We find that loss of DUOX2 activity results in transient congenital hypothyroidism and that transient congenital hypothyroidism caused by DUOX2 mutations is inherited as an autosomal recessive trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691062.RADPlvignQl318jbjbhk0j7T_oZ0HWeY5FVoxwZ32H-Jo130_provenance.
- NP691061.RAaXMgAQ55bDTiBQKEQq5YAQSJftjaQ5jK1AFPtT8x8yM130_assertion description "[We find that loss of DUOX2 activity results in transient congenital hypothyroidism and that transient congenital hypothyroidism caused by DUOX2 mutations is inherited as an autosomal recessive trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691061.RAaXMgAQ55bDTiBQKEQq5YAQSJftjaQ5jK1AFPtT8x8yM130_provenance.
- NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_assertion description "[We find that loss of DUOX2 activity results in transient congenital hypothyroidism and that transient congenital hypothyroidism caused by DUOX2 mutations is inherited as an autosomal recessive trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_provenance.
- NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_assertion description "[We find that loss of DUOX2 activity results in transient congenital hypothyroidism and that transient congenital hypothyroidism caused by DUOX2 mutations is inherited as an autosomal recessive trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_provenance.