Matches in Nanopublications for { ?s ?p "[Currently, MHA, SBS, FTNS and EPS are considered to be distinct clinical manifestation of a single illness caused by mutations of the MYH9 gene encoding the heavy chain of non-muscle myosin IIA (NMMHC-IIA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_assertion description "[Currently, MHA, SBS, FTNS and EPS are considered to be distinct clinical manifestation of a single illness caused by mutations of the MYH9 gene encoding the heavy chain of non-muscle myosin IIA (NMMHC-IIA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_provenance.
- NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_assertion description "[Currently, MHA, SBS, FTNS and EPS are considered to be distinct clinical manifestation of a single illness caused by mutations of the MYH9 gene encoding the heavy chain of non-muscle myosin IIA (NMMHC-IIA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_provenance.
- NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_assertion description "[Currently, MHA, SBS, FTNS and EPS are considered to be distinct clinical manifestation of a single illness caused by mutations of the MYH9 gene encoding the heavy chain of non-muscle myosin IIA (NMMHC-IIA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_provenance.
- NP576743.RAKWls95QIcqzdCtyO6mw5tGjIUbV15aNZ2NknWxgi3oE130_assertion description "[Currently, MHA, SBS, FTNS and EPS are considered to be distinct clinical manifestation of a single illness caused by mutations of the MYH9 gene encoding the heavy chain of non-muscle myosin IIA (NMMHC-IIA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576743.RAKWls95QIcqzdCtyO6mw5tGjIUbV15aNZ2NknWxgi3oE130_provenance.
- NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_assertion description "[Currently, MHA, SBS, FTNS and EPS are considered to be distinct clinical manifestation of a single illness caused by mutations of the MYH9 gene encoding the heavy chain of non-muscle myosin IIA (NMMHC-IIA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_provenance.