Matches in Nanopublications for { ?s ?p "[BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Bj�rnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP435891.RADeUbKm0uAHmpfybfIbZ9Ec-zWq56EgwQmSeRsyzuds0130_assertion description "[BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Bj�rnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435891.RADeUbKm0uAHmpfybfIbZ9Ec-zWq56EgwQmSeRsyzuds0130_provenance.
- NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_assertion description "[BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Bj�rnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_provenance.
- NP595180.RAc6SdamQ_RrwAtgNTvHZ9vT4xau0A-RDSBcCWpFFjzes130_assertion description "[BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Bj�rnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595180.RAc6SdamQ_RrwAtgNTvHZ9vT4xau0A-RDSBcCWpFFjzes130_provenance.
- NP595181.RAY-ZbqxOPQ4mG31NCC7zrL8M4lGj0t8ppjL_OnzzZbUw130_assertion description "[BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Bj�rnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595181.RAY-ZbqxOPQ4mG31NCC7zrL8M4lGj0t8ppjL_OnzzZbUw130_provenance.
- NP595179.RAuvedFpL8e9PNry7bhxnpOGvYtAnNQh0CYHzxjn_Y9uU130_assertion description "[BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Bj�rnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595179.RAuvedFpL8e9PNry7bhxnpOGvYtAnNQh0CYHzxjn_Y9uU130_provenance.
- NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_assertion description "[BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Bj�rnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_provenance.
- NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_assertion description "[BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Bj�rnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_provenance.
- NP265980.RAMSnVaNuMqQeFtjz-7sQzQiQyqmpE7QjVEU97AUV--5Q130_assertion description "[BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Bj�rnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265980.RAMSnVaNuMqQeFtjz-7sQzQiQyqmpE7QjVEU97AUV--5Q130_provenance.
- NP265994.RAFgNr9mFR_e2Zh6MZUsmXfb5aXEuhYltAeUGfOmig-vY130_assertion description "[BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Bj�rnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265994.RAFgNr9mFR_e2Zh6MZUsmXfb5aXEuhYltAeUGfOmig-vY130_provenance.