Matches in Nanopublications for { ?s ?p "[Independently, another group has recently observed SRD5A3 mutations in several families with a type 1 congenital disorder of glycosylation (CDG type Ix, OMIM 212067), mental retardation, cerebellar ataxia and eye disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP645759.RA9T2bWjm0c9aFhvFjcRoop0TjHSpQGB4Tac19hxILmRA130_assertion description "[Independently, another group has recently observed SRD5A3 mutations in several families with a type 1 congenital disorder of glycosylation (CDG type Ix, OMIM 212067), mental retardation, cerebellar ataxia and eye disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645759.RA9T2bWjm0c9aFhvFjcRoop0TjHSpQGB4Tac19hxILmRA130_provenance.
- NP944663.RASeFLE3AYC1WrDFBBgAjO_0FI6JOhyeL4mOgeHlDjXFs130_assertion description "[Independently, another group has recently observed SRD5A3 mutations in several families with a type 1 congenital disorder of glycosylation (CDG type Ix, OMIM 212067), mental retardation, cerebellar ataxia and eye disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP944663.RASeFLE3AYC1WrDFBBgAjO_0FI6JOhyeL4mOgeHlDjXFs130_provenance.
- assertion description "[Independently, another group has recently observed SRD5A3 mutations in several families with a type 1 congenital disorder of glycosylation (CDG type Ix, OMIM 212067), mental retardation, cerebellar ataxia and eye disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP915320.RAJWU_GReLQHNmvjxPHVDJwNG8rIQHnuDoHRm5jtMrTmU130_assertion description "[Independently, another group has recently observed SRD5A3 mutations in several families with a type 1 congenital disorder of glycosylation (CDG type Ix, OMIM 212067), mental retardation, cerebellar ataxia and eye disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915320.RAJWU_GReLQHNmvjxPHVDJwNG8rIQHnuDoHRm5jtMrTmU130_provenance.
- NP832086.RA1VZ0kn1mzb2dR4Vmuvu034LG2d6R-4fgNQ2XnaqmBps130_assertion description "[Independently, another group has recently observed SRD5A3 mutations in several families with a type 1 congenital disorder of glycosylation (CDG type Ix, OMIM 212067), mental retardation, cerebellar ataxia and eye disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP832086.RA1VZ0kn1mzb2dR4Vmuvu034LG2d6R-4fgNQ2XnaqmBps130_provenance.
- NP944664.RA7znYy4t-gtmWI3HtwbxF7goJwhQkhv6ViJs2PYAnGx8130_assertion description "[Independently, another group has recently observed SRD5A3 mutations in several families with a type 1 congenital disorder of glycosylation (CDG type Ix, OMIM 212067), mental retardation, cerebellar ataxia and eye disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP944664.RA7znYy4t-gtmWI3HtwbxF7goJwhQkhv6ViJs2PYAnGx8130_provenance.