Novel human pathological mutations. Gene symbol: SLC4A11. Disease: Corneal endothelial dystrophy 2.

Human genetics

Volumn 127, Issue 1, 2010, Pages 110-

  Chai, Shu Ming ^a   Vithana, Eranga N ^a   Venkataraman, Divya ^a   Saleh, Huda ^a   Chekkalichintavida, Najeeb P P ^a   al Sayyed, Fathi ^a   Aung, Tin ^a  

^a Third Hospital Avenue ^*  (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

ANION TRANSPORT PROTEIN; ANTIPORTER; SLC4A11 PROTEIN, HUMAN;

ARAB; ARTICLE; CODON; CONGENITAL CORNEA DYSTROPHY; CONSANGUINITY; CORNEA ENDOTHELIUM; FAMILY HEALTH; FEMALE; GENETICS; HUMAN; MALE; MISSENSE MUTATION; PATHOLOGY; QATAR;

ANION TRANSPORT PROTEINS; ANTIPORTERS; ARABS; CODON; CONSANGUINITY; CORNEAL DYSTROPHIES, HEREDITARY; ENDOTHELIUM, CORNEAL; FAMILY HEALTH; FEMALE; HUMANS; MALE; MUTATION, MISSENSE; QATAR;

EID: 77449127948     PISSN: None     EISSN: 14321203     Source Type: Journal    
DOI: None     Document Type: Article

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