Syndromic and non-syndromic deafness, molecular aspects of Pendred syndrome and its reported mutations.

Journal of Ayub Medical College, Abbottabad : JAMC

Volumn 15, Issue 3, 2003, Pages 59-64

  Shaukat, Shahzad ^a   Fatima, Zareen ^a   Zehra, Uruj ^a   Waqar, Ahmed Bilal ^a  

^a UNIVERSITY OF THE PUNJAB   (Pakistan)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; SLC26A4 PROTEIN, HUMAN;

GENETIC LINKAGE; GENETICS; GOITER; HEARING IMPAIRMENT; HUMAN; MUTATION; ONSET AGE; RECESSIVE GENE; REVIEW; SYNDROME; TRANSPORT AT THE CELLULAR LEVEL;

AGE OF ONSET; BIOLOGICAL TRANSPORT; CARRIER PROTEINS; DEAFNESS; GENES, RECESSIVE; GOITER; HUMANS; LINKAGE (GENETICS); MEMBRANE TRANSPORT PROTEINS; MUTATION; SYNDROME;

EID: 1342311539     PISSN: 10259589     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (41)