A novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema-distichiasis syndrome associated with renal disease and diabetes mellitus.

American journal of medical genetics. Part A

Volumn 131, Issue 3, 2004, Pages 281-286

  Yildirim Toruner, Cagri ^a   Subramanian, Kavitha ^a   El Manjra, Lamya ^a   Chen, Emily ^a   Goldstein, Stanley ^a   Vitale, Emilia ^a  

^a UNIVERSITY OF MEDICINE AND DENTISTRY OF NEW JERSEY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; DNA BINDING PROTEIN; FORKHEAD TRANSCRIPTION FACTOR; PRIMER DNA; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR FOXC2;

5' UNTRANSLATED REGION; ARTICLE; DIABETES MELLITUS; FRAMESHIFT MUTATION; GENETIC POLYMORPHISM; GENETICS; HUMAN; KIDNEY DISEASE; LYMPHEDEMA; NUCLEOTIDE SEQUENCE; PEDIGREE; PROMOTER REGION;

5' UNTRANSLATED REGIONS; BASE SEQUENCE; DIABETES MELLITUS; DNA; DNA PRIMERS; DNA-BINDING PROTEINS; FORKHEAD TRANSCRIPTION FACTORS; FRAMESHIFT MUTATION; HUMANS; KIDNEY DISEASES; LYMPHEDEMA; PEDIGREE; POLYMORPHISM, GENETIC; PROMOTER REGIONS (GENETICS); TRANSCRIPTION FACTORS;

EID: 20744434665     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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