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2001 | 1 |
2008 | 1 |
2024 | 0 |
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Truncating mutations in FOXC2 cause multiple lymphedema syndromes.
Hum Mol Genet. 2001 May 15;10(11):1185-9. doi: 10.1093/hmg/10.11.1185.
Hum Mol Genet. 2001.
PMID: 11371511
Primary non-syndromic lymphoedema (Meige disease) is not caused by mutations in FOXC2.
Rezaie T, Ghoroghchian R, Bell R, Brice G, Hasan A, Burnand K, Vernon S, Mansour S, Mortimer P, Jeffery S, Child A, Sarfarazi M.
Rezaie T, et al.
Eur J Hum Genet. 2008 Mar;16(3):300-4. doi: 10.1038/sj.ejhg.5201982. Epub 2008 Jan 16.
Eur J Hum Genet. 2008.
PMID: 18197197
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