Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P gene.
| Autor: | Aquaron, Robert1 robert.aquaron@medecine.univ-mrs.fr, Soufir, Nadem2, Bergé-Lefranc, Jean-Louis3, Badens, Catherine4, Austerlitz, Frederic5, Grandchamp, Bernard2 |
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| Zdroj: | Journal of Human Genetics. Sep2007, Vol. 52 Issue 9, p771-780. 10p. 1 Diagram, 2 Charts. |
| Databáze: | Academic Search Ultimate |
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