Lymphedema-distichiasis and FOXC2 gene mutations

Lymphology

Volumn 34, Issue 1, 2001, Pages 1-

  Erickson, R P ^a  

^a UNIVERSITY OF ARIZONA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOPOIETIN 2; TRANSCRIPTION FACTOR;

DISTICHIASIS; EDITORIAL; EYELASH; GENE MUTATION; HAIR DISEASE; HETEROZYGOSITY; HUMAN; KNOCKOUT GENE; MILROY DISEASE; MULTIGENE FAMILY; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION;

ANIMALS; DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; FORKHEAD TRANSCRIPTION FACTORS; HUMANS; LYMPHEDEMA; MICE; MICE, KNOCKOUT; MUTATION; SYNDROME; TRANSCRIPTION FACTORS;

EID: 0034971567     PISSN: 00247766     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Editorial

References (2)

1. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome
2. Imaging documentation of arrested lymphatic development in Angiopoietin2 knockout mice