TY  - GEN
AU  - Aquaron,Robert
AU  - Soufir,Nadem
AU  - Bergé-Lefranc,Jean-Louis
AU  - Badens,Catherine
AU  - Austerlitz,Frederic
AU  - Grandchamp,Bernard
TI  - 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
SN  - 1434-5161
PY  - 2007///1109
KW  - Albinism, Oculocutaneous
KW  - genetics
KW  - Anemia, Sickle Cell
KW  - Cameroon
KW  - Case-Control Studies
KW  - Female
KW  - Gene Deletion
KW  - Genotype
KW  - Globins
KW  - Haplotypes
KW  - Homozygote
KW  - Humans
KW  - Membrane Transport Proteins
KW  - Mutation
KW  - Pedigree
KW  - Polymorphism, Single Nucleotide
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1007/s10038-007-0181-y
ER  -