Matches in Nanopublications for { ?s ?p "[The Ala4894Thr RyR1 variant was found in a Japanese patient with susceptibility to MH, and the Ala4894Pro variant in a rare case of myopathy: congenital neuromuscular disease with uniform type 1 fiber (CNMDU1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_assertion description "[The Ala4894Thr RyR1 variant was found in a Japanese patient with susceptibility to MH, and the Ala4894Pro variant in a rare case of myopathy: congenital neuromuscular disease with uniform type 1 fiber (CNMDU1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_provenance.
- NP570967.RA6bc6HHpLRVYlLUfJZw-YWNFdYFd4PW7Bxxl7DEon3V0130_assertion description "[The Ala4894Thr RyR1 variant was found in a Japanese patient with susceptibility to MH, and the Ala4894Pro variant in a rare case of myopathy: congenital neuromuscular disease with uniform type 1 fiber (CNMDU1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570967.RA6bc6HHpLRVYlLUfJZw-YWNFdYFd4PW7Bxxl7DEon3V0130_provenance.