In Silico approach for identification, prediction of AMPD1 gene nsSNPs associated with Myoadenylate Deaminase deficiency

Background: Myoadenylate deaminase deficiency is an autosomal recessive metabolic myopathy caused by mutations in the Adenosine monophosphate deaminase 1 gene. Adenosine monophosphate deaminase 1 gene deficiency is one of the most common causes of exercise-induced myopathy. In this study, non-synony...

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Hlavní autoři:	Abrar Mohamed, Abdelrahman Hamza, Hiba Fadl, Afra Albkrye, Hadeel Ahmed, Hazem Abubaker, Sahar Elbager
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Society of Pathological Biochemistry and Hematology 2023-03-01
Edice:	Journal of Bioscience and Applied Research
Témata:	ampd1 gene myoadenylate deaminase deficiency myopathy bioinformatics nssnps & in silico
On-line přístup:	https://jbaar.journals.ekb.eg/article_284727_c155d2c5a19d2673646e9e312582b6b0.pdf
Tagy:	Přidat tag Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!