EDITORIAL
Published on 14 Mar 2022
Editorial: Inherited Protein Glycosylation Defects in Humans
doi 10.3389/fgene.2022.851438
- 920 views
- Frontiers in Genetics
- Genetics of Common and Rare Diseases
- Research Topics
- Inherited Protein Glycosylation Defects in Human Diseases
Inherited Protein Glycosylation Defects in Human Diseases
16k
Total Downloads
72k
Total Views and Downloads
Submit your idea
Select the journal/section where you want your idea to be submitted:
Articles
ORIGINAL RESEARCH
Published on 08 Dec 2021
Fatal Neonatal DOLK-CDG as a Rare Form of Syndromic Ichthyosis
doi 10.3389/fgene.2021.719624
- 1,927 views
- 5 citations
ORIGINAL RESEARCH
Published on 01 Dec 2021
SRD5A3-CDG: Emerging Phenotypic Features of an Ultrarare CDG Subtype
doi 10.3389/fgene.2021.737094
- 3,508 views
- 12 citations
BRIEF RESEARCH REPORT
Published on 11 Oct 2021
Stroke-Like Episodes in PMM2-CDG: When the Lack of Other Evidence Is the Only Evidence
doi 10.3389/fped.2021.717864
- 3,080 views
- 7 citations
ORIGINAL RESEARCH
Published on 17 Sep 2021
Development and Initial Characterization of Cellular Models for COG Complex-Related CDG-II Diseases
doi 10.3389/fgene.2021.733048
- 2,711 views
- 16 citations
REVIEW
Published on 10 Sep 2021
Treatment Options in Congenital Disorders of Glycosylation
doi 10.3389/fgene.2021.735348
- 9,624 views
- 17 citations
ORIGINAL RESEARCH
Published on 09 Sep 2021
ALG1-CDG Caused by Non-functional Alternative Splicing Involving a Novel Pathogenic Complex Allele
doi 10.3389/fgene.2021.744884
- 2,735 views
- 4 citations
REVIEW
Published on 03 Sep 2021
Congenital Disorders of Glycosylation: What Clinicians Need to Know?
doi 10.3389/fped.2021.715151
- 12,667 views
- 32 citations
MINI REVIEW
Published on 03 Sep 2021
GM1 Gangliosidosis—A Mini-Review
doi 10.3389/fgene.2021.734878
- 22,323 views
- 53 citations
ORIGINAL RESEARCH
Published on 10 Aug 2021
The Estimated Prevalence of N-Linked Congenital Disorders of Glycosylation Across Various Populations Based on Allele Frequencies in General Population Databases
doi 10.3389/fgene.2021.719437
- 3,888 views
- 15 citations
ORIGINAL RESEARCH
Published on 03 Aug 2021
Phenotype and Genotype Study of Chinese POMT2-Related α-Dystroglycanopathy
doi 10.3389/fgene.2021.692479
- 2,384 views
- 6 citations
ORIGINAL RESEARCH
Published on 05 Jul 2021
Liver Involvement in Congenital Disorders of Glycosylation and Deglycosylation
doi 10.3389/fped.2021.696918
- 3,317 views
- 6 citations
Published in
Frontiers in Genetics
- Genetics of Common and Rare Diseases
Participating Journals
Frontiers in Pediatrics
- 2.1 impact factor
- 3.6 citescore
Impact
- 72kTopic views
- 54kArticle views
- 16kArticle downloads