Gene symbol: CMD1J. Disease: SensoriNeural Hearing Loss (SNHL).

Human genetics

Volumn 117, Issue 2-3, 2005, Pages 297-

  Arbustini Eloisa, A E ^a   Diegoli, M ^a   Pasotti, M ^a   Grasso, M ^a   Marziliano, N ^a   De Donato, G ^a  

^a FONDAZIONE IRCCS POLICLINICO SAN MATTEO   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; TCF21 PROTEIN, HUMAN; TRANSCRIPTION FACTOR;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CODON; FEMALE; GENETICS; HUMAN; PERCEPTION DEAFNESS; POINT MUTATION; CHILD; CONGESTIVE CARDIOMYOPATHY;

ADULT; AMINO ACID SUBSTITUTION; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; CODON; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; POINT MUTATION; TRANSCRIPTION FACTORS; CARDIOMYOPATHY, DILATED; CHILD;

EID: 26944491544     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)