Matches in Nanopublications for { ?s ?p "[In summary, missense mutations within the exons of the androgen receptor gene encoding the steroid-binding domain of the receptor are common causes of both partial and complete forms of androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[In summary, missense mutations within the exons of the androgen receptor gene encoding the steroid-binding domain of the receptor are common causes of both partial and complete forms of androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[In summary, missense mutations within the exons of the androgen receptor gene encoding the steroid-binding domain of the receptor are common causes of both partial and complete forms of androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_assertion description "[In summary, missense mutations within the exons of the androgen receptor gene encoding the steroid-binding domain of the receptor are common causes of both partial and complete forms of androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_provenance.
- NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_assertion description "[In summary, missense mutations within the exons of the androgen receptor gene encoding the steroid-binding domain of the receptor are common causes of both partial and complete forms of androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_provenance.
- NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_assertion description "[In summary, missense mutations within the exons of the androgen receptor gene encoding the steroid-binding domain of the receptor are common causes of both partial and complete forms of androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313553.RALbdu0L4-VB6pSfuInw1gOSxcs3eE7fMfLZ0vTe2cZY8130_provenance.