Matches in Nanopublications for { ?s ?p "[The peripheral myelin protein 22 mutation W28R was associated with CMT1 and profound deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_assertion description "[The peripheral myelin protein 22 mutation W28R was associated with CMT1 and profound deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_provenance.
- NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_assertion description "[The peripheral myelin protein 22 mutation W28R was associated with CMT1 and profound deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_provenance.
- NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_assertion description "[The peripheral myelin protein 22 mutation W28R was associated with CMT1 and profound deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_provenance.
- NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_assertion description "[The peripheral myelin protein 22 mutation W28R was associated with CMT1 and profound deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_provenance.