Write a 7-10-page report on the biochemistry of an inherited disease.

The written report should be 7-10-page paper long (double spaced, 1-inch margins, no headings). The report may include a maximum of 4 figures or tables. Each figure or table should not cover more than 1/3 of the page and be accompanied by a legend to thoroughly communicate what is in the figure.

This written assignment should talk about the biochemistry and metabolic consequences of a monogenic, inherited disease.

Generally, these diseases involve the mutation of a single gene that encodes for an enzyme or transporter. Choosing a disease whose biochemical details have been at least partly worked out will make gathering information much easier.

Include the gene mutated and the function of the encoded protein (when not mutated) for each disease.

Please use scientific journal articles and not websites as your primary source of information. Using at least ten references is a reasonable goal. Sources published within the last 5 years will provide the most up to date information and should be used whenever possible.

The best place to start your search about the material/source is to look for reviews at the National library of Medicine website {(https://pubmed.ncbi.nlm.nih.gov/) (please narrow down your search criteria to reviews only)}. Please cite references as done in the Journal of Biological Chemistry {(https://www.jbc.org/content/authorinfo) (please check under references section)}. The reports should center on biochemistry and not pathology.

Write a 7-10-page report on the biochemistry of an inherit...