Matches in Nanopublications for { ?s ?p "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 11 of
11
with 100 items per page.
- NP255605.RArX19El0qxgJ3syeWJVttMFx9uF_BzMrHHO-K2EXx6TU130_assertion description "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255605.RArX19El0qxgJ3syeWJVttMFx9uF_BzMrHHO-K2EXx6TU130_provenance.
- NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_assertion description "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_provenance.
- NP502061.RAfJ3iw81fnuiFI-fuqgSthacRe9qYxzv9_ULRpWHW5h4130_assertion description "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502061.RAfJ3iw81fnuiFI-fuqgSthacRe9qYxzv9_ULRpWHW5h4130_provenance.
- NP439323.RAzYM3vy3jhfZ02piJpUsYpWWlApxA_LYCajCPgxfUm9s130_assertion description "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439323.RAzYM3vy3jhfZ02piJpUsYpWWlApxA_LYCajCPgxfUm9s130_provenance.
- assertion description "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP588174.RADeHcbiT-UQSu5J_hqNPbczskmChdgbtJm3t32tUgIpA130_assertion description "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588174.RADeHcbiT-UQSu5J_hqNPbczskmChdgbtJm3t32tUgIpA130_provenance.
- NP827231.RAs5cXVsImFbkZ6aREbW_n5ucPSnx8HcGyc-K1JEuC4aI130_assertion description "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827231.RAs5cXVsImFbkZ6aREbW_n5ucPSnx8HcGyc-K1JEuC4aI130_provenance.
- NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_assertion description "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_provenance.
- NP868087.RAK7-iYKkd3YeGSN4H8KnREpmwYnRHoaRK2QeNERpRxPI130_assertion description "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868087.RAK7-iYKkd3YeGSN4H8KnREpmwYnRHoaRK2QeNERpRxPI130_provenance.
- NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_assertion description "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_provenance.