Monoallelic SH2B1 Variants in Neurodevelopmental Disorders: Phenotypic Expansion and Functional Characterization of Rare Variants.

Xu X, Yuan G, Zheng B, Wang C, Zhou W, Huang S, Du S, He Y

DOI: 10.1002/mgg3.70306
Published: 2026 Sep
Container: Molecular genetics & genomic medicine
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1002/mgg3.70306,
  title = {Monoallelic SH2B1 Variants in Neurodevelopmental Disorders: Phenotypic Expansion and Functional Characterization of Rare Variants.},
  author = {Xu X and Yuan G and Zheng B and Wang C and Zhou W and Huang S and Du S and He Y},
  year = {2026},
  journal = {Molecular genetics \& genomic medicine},
  doi = {10.1002/mgg3.70306},
  url = {https://doi.org/10.1002/mgg3.70306}
}

RIS

TY  - JOUR
TI  - Monoallelic SH2B1 Variants in Neurodevelopmental Disorders: Phenotypic Expansion and Functional Characterization of Rare Variants.
AU  - Xu X
AU  - Yuan G
AU  - Zheng B
AU  - Wang C
AU  - Zhou W
AU  - Huang S
AU  - Du S
AU  - He Y
PY  - 2026
JO  - Molecular genetics & genomic medicine
DO  - 10.1002/mgg3.70306
UR  - https://doi.org/10.1002/mgg3.70306
ER  -

APA

X, X., G, Y., B, Z., C, W., W, Z., S, H., S, D., & Y, H. (2026). Monoallelic SH2B1 Variants in Neurodevelopmental Disorders: Phenotypic Expansion and Functional Characterization of Rare Variants.. Molecular genetics & genomic medicine. https://doi.org/10.1002/mgg3.70306

Source records

pubmed · retrieved 2026-09-25T04:05:21.637Z