Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online.

Human mutation

Volumn 28, Issue 5, 2007, Pages 522-523

  Ramprasad, Vedam L ^a   Ebenezer, Neil D ^a   Aung, Tin ^a   Rajagopal, Rama ^a   Yong, Victor H K ^a   Tuft, Stephen J ^a   Viswanathan, Deepa ^a   El Ashry, Mohamed F ^a   Liskova, Petra ^a   Tan, Donald T H ^a   Bhattacharya, Shomi S ^a   Kumaramanickavel, Govindasamy ^a   Vithana, Eranga N ^a  

^a VISION RESEARCH FOUNDATION   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ANION TRANSPORT PROTEIN; ANTIPORTER; SLC4A11 PROTEIN, HUMAN; UNCLASSIFIED DRUG;

ARTICLE; CORNEA DISEASE; GENETICS; HETEROZYGOTE DETECTION; HUMAN; INDIA; MUTATION; RECESSIVE GENE; UNITED STATES;

ANION TRANSPORT PROTEINS; ANTIPORTERS; CORNEAL DISEASES; GENES, RECESSIVE; HETEROZYGOTE DETECTION; HUMANS; INDIA; MUTATION; UNITED STATES;

EID: 34250648499     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9487     Document Type: Article

References (0)