ALBIN Mutation
The Albinism is a congenital anomaly and hereditary due to a defect of a pigment, the melanina, and is characterized from skin and plume much white, and red eyes. The eumelanina and the feomelanina are completely absent giving to the subject a phenotype entire white. Only red of the mask and the yellow of the bars andirons do not are interested from this phenomenon. The albinism is autosomico-recessive mutation.
MALE ALBINO × FEMALE ALBINO
In these couplings, the phenotype distinction of the bearers is possible only with the test of ulterior couplings.
