- 4.8Impact Factor
- 9.2CiteScore
- 20 daysTime to First Decision
Biomolecules, Volume 12, Issue 7
July 2022 - 152 articles
Cover Story: Galactosemia is a rare autosomal recessive metabolic disease, potentially lethal, that affects the body’s ability to metabolize galactose, a sugar found mainly in milk. Several countries have recently introduced galactosemia into their newborn screening programs. There are four types of galactosemia, depending on which enzyme of the Leloir pathway does not work. In recent years, various therapeutic approaches have been studied to provide better treatment, such as gene-based therapies and small molecules. View this paper
- Issues are regarded as officially published after their release is announced to the table of contents alert mailing list .
- You may sign up for email alerts to receive table of contents of newly released issues.
- PDF is the official format for papers published in both, html and pdf forms. To view the papers in pdf format, click on the "PDF Full-text" link, and use the free Adobe Reader to open them.
Articles
There are no articles in this issue yet.
Get Alerted
Add your email address to receive forthcoming issues of this journal.
Biomolecules - ISSN 2218-273X