Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies

Nature Genetics

Volumn 18, Issue 4, 1998, Pages 382-384

  Warner, L E ^a   Mancias, P ^a   Butler, I J ^a   McDonald, C M ^a   Keppen, L ^a   Koob, K G ^a   Lupski, J R ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR; ZINC FINGER PROTEIN;

ARTICLE; FEMALE; GENE MAPPING; GENETIC HETEROGENEITY; GENETIC LINKAGE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; INFANTILE HYPOTONIA; MAJOR CLINICAL STUDY; MALE; MARKER GENE; MISSENSE MUTATION; MOLECULAR CLONING; MYELINATION; NERVE CELL DIFFERENTIATION; PEDIGREE ANALYSIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; SEQUENCE ANALYSIS; STRUCTURE ACTIVITY RELATION; TRANSCRIPTION REGULATION;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; CHARCOT-MARIE-TOOTH DISEASE; DEMYELINATING DISEASES; DNA; DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; EARLY GROWTH RESPONSE PROTEIN 2; FAMILY HEALTH; FEMALE; GENES; HUMANS; IMMEDIATE-EARLY PROTEINS; MALE; PEDIGREE; POINT MUTATION; SEQUENCE HOMOLOGY, AMINO ACID; TRANSCRIPTION FACTORS; ZINC FINGERS;

EID: 0031943222     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0498-382     Document Type: Article

References (30)