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- NP676911.RAGU9o_vfd5nkJhm_Ayfm68Op428XVlUjRfn2aedh7MnM130_assertion type Assertion NP676911.RAGU9o_vfd5nkJhm_Ayfm68Op428XVlUjRfn2aedh7MnM130_head.
- NP676911.RAGU9o_vfd5nkJhm_Ayfm68Op428XVlUjRfn2aedh7MnM130_assertion description "[Although a clinical overlap between patients with dominant and recessive RYR1 mutations exists, in most cases with recessive mutations the pattern of muscle weakness is remarkably different from that observed in dominant CCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676911.RAGU9o_vfd5nkJhm_Ayfm68Op428XVlUjRfn2aedh7MnM130_provenance.
- NP676911.RAGU9o_vfd5nkJhm_Ayfm68Op428XVlUjRfn2aedh7MnM130_assertion evidence source_evidence_literature NP676911.RAGU9o_vfd5nkJhm_Ayfm68Op428XVlUjRfn2aedh7MnM130_provenance.
- NP676911.RAGU9o_vfd5nkJhm_Ayfm68Op428XVlUjRfn2aedh7MnM130_assertion SIO_000772 17483490 NP676911.RAGU9o_vfd5nkJhm_Ayfm68Op428XVlUjRfn2aedh7MnM130_provenance.
- NP676911.RAGU9o_vfd5nkJhm_Ayfm68Op428XVlUjRfn2aedh7MnM130_assertion wasDerivedFrom befree-20150227 NP676911.RAGU9o_vfd5nkJhm_Ayfm68Op428XVlUjRfn2aedh7MnM130_provenance.
- NP676911.RAGU9o_vfd5nkJhm_Ayfm68Op428XVlUjRfn2aedh7MnM130_assertion wasGeneratedBy ECO_0000203 NP676911.RAGU9o_vfd5nkJhm_Ayfm68Op428XVlUjRfn2aedh7MnM130_provenance.