In Silico Study of Human Gap Junction Beta-2 Protein by Homology Modeling
نویسندگان
چکیده
منابع مشابه
In Silico Study of Human Gap Junction Beta-2 Protein by Homology Modeling
Asp66his, Asp54Lys, and Asp50Asn are mutations in connexin 26 that are observed in the clinic and give rise to autosomal dominant syndromes. They are the result of point mutations in the human gap junction β-2 gene. In order to investigate the structural mechanism of Bart-Pumphrey Syndrome, Keratitis-Ichthyosis-Deafness Syndrome, and Vohwinkel Syndrome, homology modeling was carried out. Asp66 ...
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ژورنال
عنوان ژورنال: Genomics & Informatics
سال: 2010
ISSN: 1598-866X
DOI: 10.5808/gi.2010.8.2.070