Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE.

Journal of medical genetics

Volumn 37, Issue 11, 2000, Pages

  Masmoudi, S ^a   Elgaied Boulila, A ^a   Kassab, I ^a   Ben Arab, S ^a   Blanchard, S ^a   Bouzouita, J E ^a   Drira, M ^a   Kassab, A ^a   Hachicha, S ^a   Petit, C ^a   Ayadi, H ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; GAP JUNCTION PROTEIN;

GENE FREQUENCY; GENETICS; HETEROZYGOTE; HUMAN; LETTER; METHODOLOGY; NUCLEOTIDE SEQUENCE; PERCEPTION DEAFNESS; POLYACRYLAMIDE GEL ELECTROPHORESIS; PREVALENCE; TUNISIA;

CONNEXINS; DNA MUTATIONAL ANALYSIS; ELECTROPHORESIS, POLYACRYLAMIDE GEL; GENE FREQUENCY; HEARING LOSS, SENSORINEURAL; HETEROZYGOTE; HUMANS; PREVALENCE; TUNISIA;

MLCS; MLOWN;

EID: 0034324676     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.37.11.e39     Document Type: Letter

References (0)