The SOX10 transcription factor: Evaluation as a candidate gene for central and peripheral hereditary myelin disorders

Journal of Neurology

Volumn 248, Issue 6, 2001, Pages 496-499

  Pingault, V ^a   Bondurand, N ^a   Le Caignec, C ^a   Tardieu, S ^b   Lemort, N ^a   Dubourg, O ^b   Le Guern, E ^b   Goossens, M ^a   Boespflug Tanguy, O ^c  

^a HENRI MONDOR HOSPITAL   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c INSERM   (France)

Author keywords

Charcot Marie Tooth Disease; Leukodystrophy; Myelin disorders; Pelizaeus Merzbacher Disease; Sox10

Indexed keywords

TRANSCRIPTION FACTOR;

ARTICLE; DEMYELINATION; DEPIGMENTATION; GENE MUTATION; HEARING IMPAIRMENT; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; LEUKODYSTROPHY; MAJOR CLINICAL STUDY; MYELIN DEFICIENCY; NEURAL CREST; PELIZAEUS MERZBACHER DISEASE; PRIORITY JOURNAL;

EID: 0034917527     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004150170159     Document Type: Article

References (16)

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3. Myelin deficiencies in both the central and the peripheral nervous systems associated with a SOX10 mutation
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5. Proteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher Disease: Duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not
6. Charcot-Marie-Tooth disease: Lessons in genetic mechanisms
7. Childhood ataxia with diffuse central nervous system hypomyelination
8. Alexander's disease: Clues to diagnosis
9. Leukoencephalopathy with swelling and a discrepantly mild clinical course in eight children
10. Expression of the SOX 10 gene during human development
11. Neurological phenotype in Waardenburg type 4 syndrome correlates with novel SOX10 truncating mutations and expression in developing brain
12. Cooperative function of POU proteins and SOX proteins in glial cells
13. Axonal swelling and degeneration in mice ladking the major proteolipid of myelin
14. X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein gene locus
15. Protein zero gene expression is regulated by the glial transcription factor Sox10
16. Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: A developmental "neural crest syndrome" related to a SOX10 mutation