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A novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema-distichiasis syndrome associated with renal disease and diabetes mellitus
Cagri Yildirim-Toruner, Kavitha Subramanian, Lamya El Manjra, Emily Chen, Stanley Goldstein, Emilia VitaleVolume:
131A
Year:
2004
Language:
english
Pages:
6
DOI:
10.1002/ajmg.a.30390
File:
PDF, 208 KB
english, 2004