Aquaron, Robert <br/><br/>
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.  [electronic resource] 

 -  Journal of human genetics  2007 
 - 771-780 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1434-5161 
<br/><br/><label>Standard No.: </label>10.1007/s10038-007-0181-y  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Albinism, Oculocutaneous--genetics<br/>Anemia, Sickle Cell--genetics<br/>Cameroon<br/>Case-Control Studies<br/>Female<br/>Gene Deletion<br/>Genotype<br/>Globins--genetics<br/>Haplotypes<br/>Homozygote<br/>Humans<br/>Membrane Transport Proteins--genetics<br/>Mutation<br/>Pedigree<br/>Polymorphism, Single Nucleotide