Mutations in theMORC2gene cause axonal Charcot–Marie–Tooth disease

Hereditary motor and sensory neuropathies: Understanding molecular pathogenesis could lead to future treatment strategies

(2015) Nivedita U. Jerath et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

PAK1-mediated MORC2 phosphorylation promotes gastric tumorigenesis

(2015) Guiling Wang et al.   Oncotarget

Charcot-Marie-Tooth disease and pathways to molecular based therapies

(2014) T. Harel et al.   CLINICAL GENETICS

Recent advances in Charcot–Marie–Tooth disease

(2014) Jonathan Baets et al.   CURRENT OPINION IN NEUROLOGY

CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis

(2014) V Fridman et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathy

(2014) A. Echaniz-Laguna et al.   NEUROLOGY

A Dominant Mutation in FBXO38 Causes Distal Spinal Muscular Atrophy with Calf Predominance

(2013) Charlotte J. Sumner et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Cytosolic functions of MORC2 in lipogenesis and adipogenesis

(2013) Beatriz Sánchez-Solana et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

Exome sequencing identifies a new mutation in SERAC1 in a patient with 3-methylglutaconic aciduria

(2013) Frederic Tort et al.   MOLECULAR GENETICS AND METABOLISM

Clinical implications of genetic advances in Charcot–Marie–Tooth disease

(2013) Alexander M. Rossor et al.   Nature Reviews Neurology

Charcot-Marie-Tooth disease: Genetic and clinical spectrum in a Spanish clinical series

(2013) R. Sivera et al.   NEUROLOGY

The TRK-Fused Gene Is Mutated in Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement

(2012) Hiroyuki Ishiura et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing

(2012) Sinead M Murphy et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy

(2012) M. B. Harms et al.   NEUROLOGY

MORC2 Signaling Integrates Phosphorylation-Dependent, ATPase-Coupled Chromatin Remodeling during the DNA Damage Response

(2012) Da-Qiang Li et al.   Cell Reports

Charcot-marie-tooth disease subtypes and genetic testing strategies

(2011) Anita S.D. Saporta et al.   ANNALS OF NEUROLOGY

A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation

(2011) Sergiu C. Blumen et al.   ANNALS OF NEUROLOGY

Reliability of the CMT neuropathy score (second version) in Charcot-Marie-Tooth disease

(2011) Sinéad M. Murphy et al.   JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM

Identification and Expression Analysis of a Novel CW-Type Zinc Finger Protein MORC2 in Cancer Cells

(2010) Gui-Ling Wang et al.   Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology

Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies

(2010) Magdalena Zimoń et al.   BRAIN

Phenotypical features of the p.R120W mutation in the GDAP1 gene causing autosomal dominant Charcot-Marie-Tooth disease

(2010) Rafael Sivera et al.   JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM

Involvement of histone deacetylation in MORC2-mediated down-regulation of carbonic anhydrase IX

(2010) Yangguang Shao et al.   NUCLEIC ACIDS RESEARCH

A Genome-wide siRNA Screen Reveals Diverse Cellular Processes and Pathways that Mediate Genome Stability

(2009) Renee D. Paulsen et al.   MOLECULAR CELL

MutL homologs in restriction-modification systems and the origin of eukaryotic MORC ATPases

(2008) Lakshminarayan M Iyer et al.   Biology Direct

Different clinical and magnetic resonance imaging features between Charcot–Marie–Tooth disease type 1A and 2A

(2008) K.W. Chung et al.   NEUROMUSCULAR DISORDERS