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pro vyhledávání: '"Maryam Hasanzadh"'
Autor:
Maryam F. Sheikolslam, Parissa Farnia, Ali Akbar Velayati, Maryam Hasanzadh, Soheila Khalizadeh, Amir M. Farahbod
Publikováno v:
The American journal of tropical medicine and hygiene. 84(4)
The autosomal recessive disorder, because of a single mutation in interferon-γ receptor-1(IFNGR1) at position -56, was found to be associated with susceptibility to leprosy in children of the same family. The existence of such heterozygous carriers