Matches in Nanopublications for { ?s ?p "[A rare, recessive form of bilateral PNH with microcephaly and severe delay is associated with mutations of the ADP-ribosylation factor guanine nucleotide-exchange factor-2 (ARFGEF2) gene, required for vesicle and membrane trafficking from the trans-Golgi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP278861.RA91QOSIyvaiF8A-3b2BVPqNo99Qxv9sex5it6R2eRex0130_assertion description "[A rare, recessive form of bilateral PNH with microcephaly and severe delay is associated with mutations of the ADP-ribosylation factor guanine nucleotide-exchange factor-2 (ARFGEF2) gene, required for vesicle and membrane trafficking from the trans-Golgi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278861.RA91QOSIyvaiF8A-3b2BVPqNo99Qxv9sex5it6R2eRex0130_provenance.
- NP847369.RAeFxnaNJR1k17XvshAkHG39VfXzsopKl4eb6jzKNXq1I130_assertion description "[A rare, recessive form of bilateral PNH with microcephaly and severe delay is associated with mutations of the ADP-ribosylation factor guanine nucleotide-exchange factor-2 (ARFGEF2) gene, required for vesicle and membrane trafficking from the trans-Golgi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847369.RAeFxnaNJR1k17XvshAkHG39VfXzsopKl4eb6jzKNXq1I130_provenance.
- NP847371.RAUQwAQLRfzw50Lzk1gKxEVLKTS0rMsq7Lwp7RMV3EbAA130_assertion description "[A rare, recessive form of bilateral PNH with microcephaly and severe delay is associated with mutations of the ADP-ribosylation factor guanine nucleotide-exchange factor-2 (ARFGEF2) gene, required for vesicle and membrane trafficking from the trans-Golgi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847371.RAUQwAQLRfzw50Lzk1gKxEVLKTS0rMsq7Lwp7RMV3EbAA130_provenance.
- NP481414.RAJXzVfSs4V8zACHh9O7cBRe1ZAMmMBdRNofiGVXbHiiU130_assertion description "[A rare, recessive form of bilateral PNH with microcephaly and severe delay is associated with mutations of the ADP-ribosylation factor guanine nucleotide-exchange factor-2 (ARFGEF2) gene, required for vesicle and membrane trafficking from the trans-Golgi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP481414.RAJXzVfSs4V8zACHh9O7cBRe1ZAMmMBdRNofiGVXbHiiU130_provenance.
- assertion description "[A rare, recessive form of bilateral PNH with microcephaly and severe delay is associated with mutations of the ADP-ribosylation factor guanine nucleotide-exchange factor-2 (ARFGEF2) gene, required for vesicle and membrane trafficking from the trans-Golgi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A rare, recessive form of bilateral PNH with microcephaly and severe delay is associated with mutations of the ADP-ribosylation factor guanine nucleotide-exchange factor-2 (ARFGEF2) gene, required for vesicle and membrane trafficking from the trans-Golgi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP548838.RApxoUH9tlOwYpfBq9icYrliy5bCOFsG9K2CCdq_EjgN4130_assertion description "[A rare, recessive form of bilateral PNH with microcephaly and severe delay is associated with mutations of the ADP-ribosylation factor guanine nucleotide-exchange factor-2 (ARFGEF2) gene, required for vesicle and membrane trafficking from the trans-Golgi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548838.RApxoUH9tlOwYpfBq9icYrliy5bCOFsG9K2CCdq_EjgN4130_provenance.
- NP548835.RAJx64e7gzKwHT9pbj9ZYf3y9b39OI4196eVLNuo7C8P4130_assertion description "[A rare, recessive form of bilateral PNH with microcephaly and severe delay is associated with mutations of the ADP-ribosylation factor guanine nucleotide-exchange factor-2 (ARFGEF2) gene, required for vesicle and membrane trafficking from the trans-Golgi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548835.RAJx64e7gzKwHT9pbj9ZYf3y9b39OI4196eVLNuo7C8P4130_provenance.