Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8469495 | Egyptian Journal of Medical Human Genetics | 2018 | 5 Pages |
Abstract
These findings suggest that the combined homozygous and heterozygous variants of each codon and the 194Trp allele are associated with the disease, however when genotypes were compared individually, the association turned out to be insignificant.
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Authors
Rouf Maqbool, Shajrul Amin, Sabhiya Majeed, Aaliya Bhat, Shayaq ul Abeer Rasool, Mudasar Nabi,