Matches in Nanopublications for { ?s ?p "[DCX mutations are responsible for almost all familial cases, 80% of sporadic female cases, and 25% of sporadic male cases of SBH, and are associated with more severe gyral and migration abnormality over the anterior brain regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[DCX mutations are responsible for almost all familial cases, 80% of sporadic female cases, and 25% of sporadic male cases of SBH, and are associated with more severe gyral and migration abnormality over the anterior brain regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_assertion description "[DCX mutations are responsible for almost all familial cases, 80% of sporadic female cases, and 25% of sporadic male cases of SBH, and are associated with more severe gyral and migration abnormality over the anterior brain regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_provenance.