Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East.
Autor: | Romdhane, Lilia1, Kefi, Rym1, Azaiez, Hela1, Halim, Nizar, Dellagi, Koussay2,3, Abdelhak, Sonia1 sonia.abdelhak@pasteur.rns.tn |
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Zdroj: | Orphanet Journal of Rare Diseases. 2012, Vol. 7 Issue 1, p52-62. 11p. 1 Diagram, 1 Map. |
Databáze: | Academic Search Ultimate |
Externí odkaz: |