Add to ORKGCharcot-Marie-Tooth disease type 2A (CMT2A) is an untreatable childhood peripheral neuropathy caused by mutations of the mitochondrial fusion protein, mitofusin (MFN) 2. Here, pharmacological activation of endogenous normal mitofusins overcame dominant inhibitory effects of CMT2A mutants in reprogrammed human patient motor neurons, reversing hallmark mitochondrial stasis and fragmentation independent of causa
Charcot-Marie-Tooth disease type 2A (CMT2A) is the most common hereditary axonal neuropathy caused b...
Abstract BACKGROUND: The axonal forms of Charcot-Marie-Tooth (CMT2) disease are a clinically and gen...
Abstract BACKGROUND: The axonal forms of Charcot-Marie-Tooth (CMT2) disease are a clinically and gen...
A causal relationship between Mitofusin (MFN) 2 gene mutations and the hereditary axonal neuropathy ...
Charcot-Marie-Tooth disease type 2A is an autosomal dominant axonal form of peripheral neuropathy ca...
Charcot-Marie-Tooth disease type 2A is an autosomal dominant axonal form of peripheral neuropathy ca...
Mitofusin 2 (MFN2) is a protein of the mitochondrial outer membrane that belongs to a family of high...
Les mitochondries forment un réseau très dynamique remodelé par deux processus antagonistes appelés ...
Mitofusin-2 (MFN2) is a mitochondrial outer-membrane protein that plays a pivotal role in mitochondr...
Charcot-Marie-Tooth disease (CMT) is the most common form of hereditary peripheral neuropathy. The m...
Charcot-Marie-Tooth disease type 2A (CMT2A) is an axonal neuropathy caused by mutations in the mitof...
Charcot-Marie-Tooth disease type 2A (CMT2A) is an axonal neuropathy caused by mutations in the mitof...
Charcot Marie Tooth Disease (CMT) 2A is a progressive peripheral motor and sensory axonal neuropathy...
Charcot-Marie-Tooth disease (CMT) is a common, hereditary, length-dependent peripheral neuropathy ro...
Abstract BACKGROUND: The axonal forms of Charcot-Marie-Tooth (CMT2) disease are a clinically and gen...
Charcot-Marie-Tooth disease type 2A (CMT2A) is the most common hereditary axonal neuropathy caused b...
Abstract BACKGROUND: The axonal forms of Charcot-Marie-Tooth (CMT2) disease are a clinically and gen...
Abstract BACKGROUND: The axonal forms of Charcot-Marie-Tooth (CMT2) disease are a clinically and gen...
A causal relationship between Mitofusin (MFN) 2 gene mutations and the hereditary axonal neuropathy ...
Charcot-Marie-Tooth disease type 2A is an autosomal dominant axonal form of peripheral neuropathy ca...
Charcot-Marie-Tooth disease type 2A is an autosomal dominant axonal form of peripheral neuropathy ca...
Mitofusin 2 (MFN2) is a protein of the mitochondrial outer membrane that belongs to a family of high...
Les mitochondries forment un réseau très dynamique remodelé par deux processus antagonistes appelés ...
Mitofusin-2 (MFN2) is a mitochondrial outer-membrane protein that plays a pivotal role in mitochondr...
Charcot-Marie-Tooth disease (CMT) is the most common form of hereditary peripheral neuropathy. The m...
Charcot-Marie-Tooth disease type 2A (CMT2A) is an axonal neuropathy caused by mutations in the mitof...
Charcot-Marie-Tooth disease type 2A (CMT2A) is an axonal neuropathy caused by mutations in the mitof...
Charcot Marie Tooth Disease (CMT) 2A is a progressive peripheral motor and sensory axonal neuropathy...
Charcot-Marie-Tooth disease (CMT) is a common, hereditary, length-dependent peripheral neuropathy ro...
Abstract BACKGROUND: The axonal forms of Charcot-Marie-Tooth (CMT2) disease are a clinically and gen...
Charcot-Marie-Tooth disease type 2A (CMT2A) is the most common hereditary axonal neuropathy caused b...
Abstract BACKGROUND: The axonal forms of Charcot-Marie-Tooth (CMT2) disease are a clinically and gen...
Abstract BACKGROUND: The axonal forms of Charcot-Marie-Tooth (CMT2) disease are a clinically and gen...