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CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F

Known as: CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2F, CMT 2F, Charcot-Marie-Tooth disease, neuronal, Type 2F 
 
National Institutes of Health

Papers overview

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2013
2013
Mutations in the small heat shock protein HSPB1 (HSP27) are a cause of axonal Charcot–Marie–Tooth neuropathy (CMT2F) and distal… Expand
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2012
2012
A key constraint in successfully obtaining an effective inoculant is overcoming difficulties in formulating a viable and user… Expand
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2011
2011
Low effectiveness of native strains remains a limitation to soybean productivity in sub-Saharan Africa; while in other countries… Expand
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Highly Cited
2007
Highly Cited
2007
Mutations in neurofilament light (NFL) subunit and small heat-shock protein B1 (HSPB1) cause autosomal-dominant axonal Charcot… Expand
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2006
2006
ABCA1 mediates the transport of cellular cholesterol and phospholipids to HDL apolipoproteins. Apolipoprotein A-I (apoA-I… Expand
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Highly Cited
2004
Highly Cited
2004
Charcot-Marie-Tooth disease (CMT) is the most common inherited neuromuscular disease and is characterized by considerable… Expand
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2004
2004
Charcot-Marie-Tooth disease (CMT) is one of the most common inherited neurological disorders with a prevalence estimated at 1… Expand
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Highly Cited
2002
Highly Cited
2002
Abstract. Charcot-Marie-Tooth (CMT) disease is the most-common form of inherited motor and sensory neuropathy. The autosomal… Expand
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2001
2001
Charcot-Marie-Tooth disease (CMT) constitutes a genetically heterogeneous group of inherited motor and sensory peripheral… Expand
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