A new mutation in GJC2 associated with subclinical leukodystrophy

A V139M Mutation Also Causes the Reversible CNS Phenotype in CMTX

(2014) Michelle Halbrich et al.   CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES

Connexin47 Protein Phosphorylation and Stability in Oligodendrocytes Depend on Expression of Connexin43 Protein in Astrocytes

(2013) D. May et al.   JOURNAL OF NEUROSCIENCE

Functional Requirement for a Highly Conserved Charged Residue at Position 75 in the Gap Junction Protein Connexin 32

(2012) Charles K. Abrams et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Pelizaeus-Merzbacher Disease, Pelizaeus-Merzbacher-Like Disease 1, and Related Hypomyelinating Disorders

(2012) Grace Hobson et al.   SEMINARS IN NEUROLOGY

Gap junctions in inherited human disorders of the central nervous system

(2011) Charles K. Abrams et al.   BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES

Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction coupling

(2011) Sameh K. Wasseff et al.   NEUROBIOLOGY OF DISEASE

Relevance of GJC2 promoter mutation in Pelizaeus-Merzbacher-like disease

(2010) Patricia Combes et al.   ANNALS OF NEUROLOGY

X-linked hereditary motor sensory neuropathy (type 1) presenting with a stroke-like episode

(2010) GEETHA ANAND et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Functional heterotypic interactions between astrocyte and oligodendrocyte connexins

(2010) Laura M. Magnotti et al.   GLIA

Oligodendrocytes in mouse corpus callosum are coupled via gap junction channels formed by connexin47 and connexin32

(2010) Marta Maglione et al.   GLIA

Transient Leukoencephalopathy Associated With X-Linked Charcot-Marie-Tooth Disease

(2010) Tena Rosser et al.   JOURNAL OF CHILD NEUROLOGY

Coexistent Central and Peripheral Nervous System Involvement in a Charcot-Marie-Tooth Syndrome X-linked Patient

(2010) Carlo Fusco et al.   JOURNAL OF CHILD NEUROLOGY

Astroglial networks: a step further in neuroglial and gliovascular interactions

(2010) Christian Giaume et al.   NATURE REVIEWS NEUROSCIENCE

Persistent CNS dysfunction in a boy with CMT1X

(2009) Carly Siskind et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations

(2008) Jennifer L. Orthmann-Murphy et al.   BRAIN

Central Nervous System Signs in X-Linked Charcot-Marie-Tooth Disease After Hyperventilation

(2008) Jayasri Srinivasan et al.   PEDIATRIC NEUROLOGY