Skip to search formSkip to main contentSkip to account menu

Charcot-Marie-Tooth Disease, Type Ib

Known as: CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1B, Charcot-Marie-Tooth Disease, Slow Nerve Conduction Type, Linked To Duffy, Hereditary Motor and Sensory Neuropathy 1B 
Charcot-Marie-Tooth disease caused by mutations in the MPZ gene (mapped to chromosome 1q23.3). It results in sensorineural peripheral neuropathy.
National Institutes of Health

Related topics

Related topics

9 relations
Autosomal dominant inheritanceFoot DeformitiesFootdropHammer Toe

Broader (1)

Charcot-Marie-Tooth Disease

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2009
Review
2009
Mitochondrial dynamics in mammalian health and disease.
The meaning of the word mitochondrion (from the Greek mitos, meaning thread, and chondros, grain) illustrates that the… 
Review
2007
Review
2007
Trends in oral health status: United States, 1988-1994 and 1999-2004.
OBJECTIVE This report presents national estimates and trends for a variety of oral health status measures for persons aged 2… 
Review
2004
Review
2004
Tooth colour: a review of the literature.
Highly Cited
2004
Highly Cited
2004
Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer.
Wnt signaling regulates embryonic pattern formation and morphogenesis of most organs. Aberrations of regulation of Wnt signaling… 
Highly Cited
2002
Highly Cited
2002
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.
The Charcot-Marie-Tooth (CMT) disorders comprise a group of clinically and genetically heterogeneous hereditary motor and sensory… 
Highly Cited
2000
Highly Cited
2000
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
A Dutch family with tooth agenesis and various combinations of cleft palate only and cleft lip and cleft palate showed a nonsense… 
Highly Cited
1997
Highly Cited
1997
Antagonistic Interactions between FGF and BMP Signaling Pathways: A Mechanism for Positioning the Sites of Tooth Formation
Highly Cited
1996
Highly Cited
1996
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
We demonstrate that a mutation in the homeobox gene, MSX1, causes a common developmental anomaly, familial tooth agenesis… 
Highly Cited
1993
Highly Cited
1993
Connexin mutations in X-linked Charcot-Marie-Tooth disease.
X-linked Charcot-Marie-Tooth disease (CMTX) is a form of hereditary neuropathy with demyelination. Recently, this disorder was… 
Highly Cited
1962
Highly Cited
1962
Comparative cleansing efficiency of manual and power brushing.
The purpose of the studies described in this report was to evaluate the efficiency of a reciprocating motion toothbrush as an… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)