A novel frameshift mutation of FOXC2 gene in a family with...

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 Vitale
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Volume:
131A
Year:
2004
Language:
english
Pages:
6
DOI:
10.1002/ajmg.a.30390
File:
PDF, 208 KB
english, 2004
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