Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease

RC Vignogna, M Allocca, M Monticelli, JW Norris… - Elife, 2022 - elifesciences.org
The most common cause of human congenital disorders of glycosylation (CDG) are
mutations in the phosphomannomutase gene PMM2, which affect protein N-linked …
被引用次数：11 相关文章
[PDF] cnr.it

[PDF][PDF] Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease

RC Vignogna, M Allocca, M Monticelli, JW Norris… - iris.cnr.it
The most common cause of human congenital disorders of glycosylation (CDG) are
mutations in the phosphomannomutase gene PMM2, which affect protein N-linked …
[PDF] unina.it

[PDF][PDF] Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease

RC Vignogna, M Allocca, M Monticelli, JW Norris… - iris.unina.it
The most common cause of human congenital disorders of glycosylation (CDG) are
mutations in the phosphomannomutase gene PMM2, which affect protein N-linked …

Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease

RC Vignogna, A Mariateresa, M Monticelli, JW Norris… - eLife, 2022 - search.proquest.com
The most common cause of human congenital disorders of glycosylation (CDG) are
mutations in the phosphomannomutase gene PMM2, which affect protein N-linked …

Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease.

RC Vignogna, M Allocca, M Monticelli, JW Norris… - Elife, 2022 - europepmc.org
The most common cause of human congenital disorders of glycosylation (CDG) are
mutations in the phosphomannomutase gene PMM2, which affect protein N-linked …
[HTML] nih.gov

[HTML][HTML] Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease

RC Vignogna, M Allocca, M Monticelli, JW Norris… - eLife, 2022 - ncbi.nlm.nih.gov
The most common cause of human congenital disorders of glycosylation (CDG) are
mutations in the phosphomannomutase gene PMM2, which affect protein N-linked …

Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease

RC Vignogna, M Allocca, M Monticelli, JW Norris… - …, 2022 - pubmed.ncbi.nlm.nih.gov
The most common cause of human congenital disorders of glycosylation (CDG) are
mutations in the phosphomannomutase gene PMM2, which affect protein N-linked …
[PDF] glanglab.com

[PDF][PDF] Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease

RC Vignogna, M Allocca, M Monticelli, JW Norris… - glanglab.com
The most common cause of human congenital disorders of glycosylation (CDG) are
mutations in the phosphomannomutase gene PMM2, which affect protein N-linked …

Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease.

RC Vignogna, M Allocca, M Monticelli, JW Norris… - eLife, 2022 - search.ebscohost.com
The most common cause of human congenital disorders of glycosylation (CDG) are
mutations in the phosphomannomutase gene PMM2, which affect protein N-linked …
[PDF] glanglab.com

[PDF][PDF] Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease

RC Vignogna, M Allocca, M Monticelli, JW Norris… - glanglab.com
The most common cause of human congenital disorders of glycosylation (CDG) are
mutations in the phosphomannomutase gene PMM2, which affect protein N-linked …