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
Zdroj: Orphanet Journal of Rare Diseases. 2012, Vol. 7 Issue 1, p52-62. 11p. 1 Diagram, 1 Map.
Databáze: Academic Search Ultimate