Related references
Note: Only part of the references are listed.Genetic and clinical aspects of Charcot-Marie-Tooth's disease
H. Skre
CLINICAL GENETICS (2010)
De novo mutations of SETBP1 cause Schinzel-Giedion syndrome
Alexander Hoischen et al.
NATURE GENETICS (2010)
Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy.
James R. Lupski et al.
NEW ENGLAND JOURNAL OF MEDICINE (2010)
Genome sequencing reveals Charcot-Marie-Tooth disease mutation
[Anonymous]
FUTURE NEUROLOGY (2010)
Targeted capture and massively parallel sequencing of 12 human exomes
Sarah B. Ng et al.
NATURE (2009)
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
Murim Choi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
Kristien Verhoeven et al.
BRAIN (2006)
Molecular genetics of autosomal-dominant axonal Charcot-Marie-Tooth disease
Stephan Zuchner et al.
NEUROMOLECULAR MEDICINE (2006)
Mutation analysis of the PMP22, MPZ, EGR2, LITAF, and GJB1 genes in Korean patients with Charcot-Marie-Tooth neuropathy type 1
H-K Park et al.
CLINICAL GENETICS (2006)
Distribution and intensity of constraint in mammalian genomic sequence
GM Cooper et al.
GENOME RESEARCH (2005)
Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease
D Botstein et al.
NATURE GENETICS (2003)