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RAB7A wt Allele

Known as: PRO2706, RAB7, Member RAS Oncogene Family Gene, CMT2B 
Human RAB7A wild-type allele is located in the vicinity of 3q21 and is approximately 89 kb in length. This allele, which encodes ras-related protein… Expand
National Institutes of Health

Papers overview

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Review
2019
Review
2019
RAB7 is a small guanosine triphosphatase (GTPase) extensively studied as regulator of vesicular trafficking. Indeed, its role is… Expand
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2017
2017
Autophagy disruption leads to neuronal damage in hypoxic–ischemic brain injury. Rab7, a member of the Rab GTPase superfamily, has… Expand
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2014
2014
Charcot–Marie–Tooth type 2B (CMT2B) disease is a hereditary motor and sensory neuropathy subtype characterized by prominent loss… Expand
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2013
2013
Charcot-Marie-Tooth type 2B (CMT2B) disease is a hereditary motor and sensory neuropathy subtype characterized by prominent loss… Expand
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2013
2013
a Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology and Center for… Expand
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2012
2012
CMT2B (Charcot-Marie-Tooth type 2B) disease is an autosomal dominant peripheral neuropathy whose onset is in the second or third… Expand
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Highly Cited
2006
Highly Cited
2006
We report a 32-year-old patient with Charcot-Marie-Tooth (CMT2B) including foot ulcerations. Genetic analysis identified a de… Expand
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2005
2005
Background: The variable clinical features of hereditary sensory and autonomic neuropathy (HSAN I) suggest heterogeneity. Some… Expand
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Highly Cited
2004
Highly Cited
2004
There are two known autosomal dominant genes for the hereditary ulcero-mutilating neuropathies: SPTLC1 (hereditary sensory… Expand
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