Application of physiological genomics to the study of hearing disorders

Journal of Physiology

Volumn 543, Issue 1, 2002, Pages 3-12

  Heller, Stefan ^a,b  

^a HARVARD MEDICAL SCHOOL   (United States)

^b MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; CONNEXIN 43; GAP JUNCTION PROTEIN; POTASSIUM CHANNEL; POTASSIUM ION; TRANSCRIPTION FACTOR;

CONTROLLED STUDY; DNA MICROARRAY; EXPRESSED SEQUENCE TAG; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; GENOMICS; HEARING DISORDER; HEARING IMPAIRMENT; HOMEOSTASIS; HUMAN; INNER EAR; METHODOLOGY; MOLECULAR GENETICS; MOUSE; NONHUMAN; PATHOPHYSIOLOGY; PRIORITY JOURNAL; REVIEW; SEQUENCE DATABASE; COCHLEA; GENETICS; PHYSIOLOGY; AGE; COCHLEAR ION HOMEOSTASIS; DNA DETERMINATION; DNA SEQUENCE; GENETIC DATABASE; GENETIC LINKAGE; MOLECULAR PATHOLOGY; MORPHOLOGY; PHYSIOLOGICAL GENOMICS; PHYSIOLOGICAL PROCESS; TISSUE REGENERATION;

COCHLEA; GENOMICS; HEARING DISORDERS; HUMAN; HUMANS;

EID: 0037101908     PISSN: 00223751     EISSN: None     Source Type: Journal    
DOI: 10.1113/jphysiol.2002.018911     Document Type: Review

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