A <i>MORC2</i> Variant Associated With Severe Intellectual Disability and Unusual Phenotype

Harry Wilton‐Clark, Kati Kämpjärvi, Oksana Suchowersky, Shailly Jain‐Ghai

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DOI: 10.1002/ajmg.a.70307
Published: 2026-09-24
Container: American Journal of Medical Genetics Part A
Publisher: Wiley
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1002/ajmg.a.70307,
  title = {A
                    <i>MORC2</i>
                    Variant Associated With Severe Intellectual Disability and Unusual Phenotype},
  author = {Harry Wilton‐Clark and Kati Kämpjärvi and Oksana Suchowersky and Shailly Jain‐Ghai},
  year = {2026},
  journal = {American Journal of Medical Genetics Part A},
  doi = {10.1002/ajmg.a.70307},
  url = {https://doi.org/10.1002/ajmg.a.70307}
}

RIS

TY  - JOUR
TI  - A
                    <i>MORC2</i>
                    Variant Associated With Severe Intellectual Disability and Unusual Phenotype
AU  - Harry Wilton‐Clark
AU  - Kati Kämpjärvi
AU  - Oksana Suchowersky
AU  - Shailly Jain‐Ghai
PY  - 2026
JO  - American Journal of Medical Genetics Part A
DO  - 10.1002/ajmg.a.70307
UR  - https://doi.org/10.1002/ajmg.a.70307
ER  -

APA

Wilton‐Clark, H., Kämpjärvi, K., Suchowersky, O., & Jain‐Ghai, S. (2026). A <i>MORC2</i> Variant Associated With Severe Intellectual Disability and Unusual Phenotype. American Journal of Medical Genetics Part A. https://doi.org/10.1002/ajmg.a.70307

Source records

crossref · retrieved 2026-09-25T11:03:41.436Z