Corrigendum: Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness (Human Molecular Genetics (2015) 24:13 (3651-3661) DOI: 10.1093/hmg/ddv109);Perinatal GJB2 gene transfer rescues hearing in a mouse model of hereditary deafness

Human Molecular Genetics

Volumn 24, Issue 13, 2015, Pages 3651-3661

  Iizuka, Takashi ^a   Kamiya, Kazusaku ^a   Gotoh, Satoru ^b   Sugitani, Yoshinobu ^b   Suzuki, Masaaki ^c   Noda, Tetsuo ^b,d   Minowa, Osamu ^b,d   Ikeda, Katsuhisa ^a  

^a JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b CANCER INSTITUTE   (Japan)

^c TEIKYO UNIVERSITY CHIBA MEDICAL CENTER   (Japan)

^d RIKEN BIORESOURCE CENTER   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; GAP JUNCTION PROTEIN;

ADULT; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; AUDITORY RESPONSE; AUDITORY THRESHOLD; BODY WEIGHT; CONTROLLED STUDY; CORTI ORGAN; FUNCTIONAL ASSESSMENT; GAP JUNCTION; GENE DELIVERY SYSTEM; GENE TRANSFER; GLUCOSE TRANSPORT; HEARING IMPAIRMENT; HEREDITARY DEAFNESS; MOUSE; NONHUMAN; OUTER HAIR CELL; PERINATAL PERIOD; PHENOTYPE; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; RANDOMIZED CONTROLLED TRIAL; SPEECH PERCEPTION; SPIRAL LIGAMENT; TIGHT JUNCTION; ANIMAL; C57BL MOUSE; COCHLEA; DEAFNESS; DEPENDOPARVOVIRUS; DISEASE MODEL; FEMALE; GENE THERAPY; GENETICS; HEARING; HUMAN; MALE; METABOLISM; PATHOPHYSIOLOGY; PERINATAL CARE;

ADENO-ASSOCIATED VIRUS; MUS;

ANIMALS; COCHLEA; CONNEXINS; DEAFNESS; DEPENDOVIRUS; DISEASE MODELS, ANIMAL; FEMALE; GENE TRANSFER TECHNIQUES; GENETIC THERAPY; HEARING; HUMANS; MALE; MICE; MICE, INBRED C57BL; PERINATAL CARE;

EID: 84936745900     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddz041     Document Type: Erratum

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