EDITORIAL
Published on 14 Aug 2023
Editorial: Deciphering the etiology of rare genetic disorders associated with protein phosphatases
doi 10.3389/fcell.2023.1241606
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- Frontiers in Cell and Developmental Biology
- Molecular and Cellular Pathology
- Research Topics
- Deciphering the Etiology of Rare Genetic Disorders Associated with Protein Phosphatases
Deciphering the Etiology of Rare Genetic Disorders Associated with Protein Phosphatases
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Articles
ORIGINAL RESEARCH
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- 1,308 views
- 1 citation
ORIGINAL RESEARCH
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- 1 citation
REVIEW
Published on 23 Jan 2023
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doi 10.3389/fcell.2022.1051311
- 5,565 views
- 1 citation
ORIGINAL RESEARCH
Published on 30 Nov 2022
Clinical and molecular characteristics of a novel rare de novo variant in PPP2CA in a patient with a developmental disorder, autism, and epilepsy
doi 10.3389/fcell.2022.1059938
- 2,483 views
- 1 citation
REVIEW
Published on 04 Nov 2022
Modeling (not so) rare developmental disorders associated with mutations in the protein-tyrosine phosphatase SHP2
doi 10.3389/fcell.2022.1046415
- 3,169 views
- 5 citations
REVIEW
Published on 13 Oct 2022
The role of serine/threonine phosphatases in human development: Evidence from congenital disorders
doi 10.3389/fcell.2022.1030119
- 4,377 views
- 8 citations
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Frontiers in Cell and Developmental Biology
- Molecular and Cellular Pathology
- Cellular Biochemistry
Participating Journals
Frontiers in Chemistry
Cellular BiochemistryOffline
- 3.8 impact factor
- 8.5 citescore
Frontiers in Molecular Biosciences
- 3.9 impact factor
- 7.2 citescore
Impact
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- 17kArticle views
- 4,710Article downloads