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CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C
Known as:
Charcot-Marie-Tooth Neuropathy, Type 4c
, Cmt4c
, Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive, Type 4c
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National Institutes of Health
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Related topics
Related topics
10 relations
Abnormality of the cranial nerves
Autosomal recessive inheritance
Facial Paresis
Foot Deformities
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Broader (1)
Charcot-Marie-Tooth Disease
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Charcot–Marie–Tooth disease type 4C in Norway: Clinical characteristics, mutation spectrum and minimum prevalence
K. Arntzen
,
Helle Høyer
,
+6 authors
T. Fagerheim
Neuromuscular Disorders
2018
Corpus ID: 51623291
2017
2017
A 11 Patent Number : 45 Date of Patent : 5 , 712 . 298 Jan . 27 , 1998
Gulden Lomberg Chemische
,
Useas Cyclc
2017
Corpus ID: 44080961
Compounds of formula (I), in which one of the substituents R1 or R2 stands for hydrogen, 1-6C-alkoxy, 3-7C cycloalkoxy, 3-7C…
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2016
2016
[Mutation analysis for a family affected with Charcot-Marie-Tooth disease type 4C].
Zhen Yu
,
Jia-ying Zhang
,
+5 authors
Ming-min Gu
Zhonghua yi xue yi chuan xue za zhi = Zhonghua…
2016
Corpus ID: 38193496
OBJECTIVE To identify potential mutation in a Chinese family affected with Charcot-Marie-Tooth disease(CMT). METHODS Clinical…
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Review
2013
Review
2013
[Current issues in hereditary neuropathies].
A. Lacour
Revue neurologique (Paris)
2013
Corpus ID: 23396916
2012
2012
공학교육혁신의 4C 구현 거점 사업
송동주
2012
Corpus ID: 179361535
2010
2010
Correction for “ SH 3 TC 2 / KIAA 1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system
Weiqing Zhanga
,
Y. Zhoua
,
Michael A. Collinsf
,
D. Zhanga
2010
Corpus ID: 14474228
CHEMISTRY Correction for “Depression of reactivity by the collision energy in the single barrier H + CD4 → HD + CD3 reaction,” by…
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2009
2009
Genetic Study of Demyelinating form of Autosomal-Recessive Charcot–Marie–Tooth Diseases in a Turkish Family
Nilufer Sahin-Calapoglu
,
M. Soyoz
,
Mustafa Calapoğlu
,
N. Ozçelik
International Journal of Neuroscience
2009
Corpus ID: 41710565
Charcot–Marie–Tooth (CMT) disease is a clinically and genetically heterogeneous group of inherited peripheral motor and sensory…
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2006
2006
N.P.3 03 Three novel mutations of the myelin Po gene (MPZ) in Portuguese families with CMT1B
T. Coelho
,
M. Santos
,
+6 authors
A. Guimarães
Neuromuscular Disorders
2006
Corpus ID: 54343455
1998
1998
CAFFEINE DEGRADATION IN LEAVES AND FRUITS OF COFFEA ARABICA AND COFFEA DEWEVREP
A. P. Vitória
,
Paulo Mazzafeiw
1998
Corpus ID: 55162836
The cofTee species Coffea dewevrei and Coffea ai-abica have marked differences in caifeine metabolism and the control of the…
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1972
1972
Hemoglobin synthesis in short-term cultures of human fetal hematopoietic tissues.
R. Basch
Blood
1972
Corpus ID: 31981585
Hemoglobin synthesis in the erythropoietic tissues of 11 normal human fetuses ranging in age from 6 to 21 wk has been studied…
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