Gap junctions in inherited human disease

Pflugers Archiv European Journal of Physiology

Volumn 460, Issue 2, 2010, Pages 451-466

  Zoidl, Georg ^a   Dermietzel, Rolf ^a  

^a RUHR UNIVERSITY BOCHUM   (Germany)

Author keywords

Channelopathy; Connexin; Gap junction; Intercellular communication

Indexed keywords

CONNEXIN 26; CONNEXIN 30; CONNEXIN 31; CONNEXIN 32; CONNEXIN 37; CONNEXIN 40; CONNEXIN 43; CONNEXIN 46; CONNEXIN 47; GAP JUNCTION PROTEIN;

BART PUMPHREY SYNDROME; CARDIOVASCULAR DISEASE; CATARACT; CELL COMMUNICATION; ERYTHROKERATODERMA FIGURATA VARIABILIS; GAP JUNCTION; GENE FUNCTION; GENE MUTATION; GENETIC DISORDER; HEARING IMPAIRMENT; HEREDITARY MOTOR SENSORY NEUROPATHY; HIDROTIC ECTODERMAL DYSPLASIA; HUMAN; HUMAN GENETICS; HYSTRIX LIKE ICHTHYOSIS DEAFNESS SYNDROME; KERATITIS ICHTHYOSIS DEAFNESS SYNDROME; KERATODERMA HEREDITARIUM MUTILANS; NONHUMAN; OCULODENTODIGITAL SYNDROME; PELIZAEUS MERZBACHER DISEASE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN STRUCTURE; REVIEW; RISK FACTOR; SKIN DISEASE;

ANIMALS; CELL COMMUNICATION; CONNEXINS; GAP JUNCTIONS; GENETIC DISEASES, INBORN; HUMANS; LABYRINTH DISEASES; MODELS, ANIMAL; PELIZAEUS-MERZBACHER DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; SKIN DISEASES;

EID: 77955570389     PISSN: 00316768     EISSN: 14322013     Source Type: Journal    
DOI: 10.1007/s00424-010-0789-1     Document Type: Review

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