Matches in Nanopublications for { ?s ?p "[We performed direct genotyping of INF2 in 16 index patients with Charcot-Marie-Tooth neuropathy and FSGS who did not have a mutation in PMP22 or MPZ, encoding peripheral myelin protein 22 and myelin protein zero, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_assertion description "[We performed direct genotyping of INF2 in 16 index patients with Charcot-Marie-Tooth neuropathy and FSGS who did not have a mutation in PMP22 or MPZ, encoding peripheral myelin protein 22 and myelin protein zero, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_provenance.
- NP948367.RAdb4TN3AcRz859o5fVa5AtPI6lqkmxhUugAXn5OND2x4130_assertion description "[We performed direct genotyping of INF2 in 16 index patients with Charcot-Marie-Tooth neuropathy and FSGS who did not have a mutation in PMP22 or MPZ, encoding peripheral myelin protein 22 and myelin protein zero, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948367.RAdb4TN3AcRz859o5fVa5AtPI6lqkmxhUugAXn5OND2x4130_provenance.
- NP632487.RAk6BTXegJuEn6JO_f5wXE9AS_71DiIfXx6FCmCPtWmIc130_assertion description "[We performed direct genotyping of INF2 in 16 index patients with Charcot-Marie-Tooth neuropathy and FSGS who did not have a mutation in PMP22 or MPZ, encoding peripheral myelin protein 22 and myelin protein zero, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632487.RAk6BTXegJuEn6JO_f5wXE9AS_71DiIfXx6FCmCPtWmIc130_provenance.
- NP568288.RAypAGGxEsZXjtZPW0AYPLuG3uzyKLDz6kPATdjialVgg130_assertion description "[We performed direct genotyping of INF2 in 16 index patients with Charcot-Marie-Tooth neuropathy and FSGS who did not have a mutation in PMP22 or MPZ, encoding peripheral myelin protein 22 and myelin protein zero, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568288.RAypAGGxEsZXjtZPW0AYPLuG3uzyKLDz6kPATdjialVgg130_provenance.
- NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_assertion description "[We performed direct genotyping of INF2 in 16 index patients with Charcot-Marie-Tooth neuropathy and FSGS who did not have a mutation in PMP22 or MPZ, encoding peripheral myelin protein 22 and myelin protein zero, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_provenance.
- NP662249.RA7RuuCPhuyxBOcNRCNEszkWnNi6m9_D-mh3ESn25La6A130_assertion description "[We performed direct genotyping of INF2 in 16 index patients with Charcot-Marie-Tooth neuropathy and FSGS who did not have a mutation in PMP22 or MPZ, encoding peripheral myelin protein 22 and myelin protein zero, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662249.RA7RuuCPhuyxBOcNRCNEszkWnNi6m9_D-mh3ESn25La6A130_provenance.
- NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_assertion description "[We performed direct genotyping of INF2 in 16 index patients with Charcot-Marie-Tooth neuropathy and FSGS who did not have a mutation in PMP22 or MPZ, encoding peripheral myelin protein 22 and myelin protein zero, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_provenance.
- NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_assertion description "[We performed direct genotyping of INF2 in 16 index patients with Charcot-Marie-Tooth neuropathy and FSGS who did not have a mutation in PMP22 or MPZ, encoding peripheral myelin protein 22 and myelin protein zero, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_provenance.