Research needs of caregivers of people with 22q11.2 deletion syndrome in Japan: A qualitative analysis.

Kanehara A, Tanaka M, Kumakura Y, Morishima R, Sawai Y, Takahashi Y, Yagishita S, Jinde S, Kasai K.

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DOI: 10.1002/pcn5.70352
Published: 2026-06-04
Container: PCN Rep
Publisher: Not recorded
Open access: no

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Cite this work

BibTeX

@article{allodium:10.1002/pcn5.70352,
  title = {Research needs of caregivers of people with 22q11.2 deletion syndrome in Japan: A qualitative analysis.},
  author = {Kanehara A and  Tanaka M and  Kumakura Y and  Morishima R and  Sawai Y and  Takahashi Y and  Yagishita S and  Jinde S and  Kasai K.},
  year = {2026},
  journal = {PCN Rep},
  doi = {10.1002/pcn5.70352},
  url = {https://doi.org/10.1002/pcn5.70352}
}

RIS

TY  - JOUR
TI  - Research needs of caregivers of people with 22q11.2 deletion syndrome in Japan: A qualitative analysis.
AU  - Kanehara A
AU  -  Tanaka M
AU  -  Kumakura Y
AU  -  Morishima R
AU  -  Sawai Y
AU  -  Takahashi Y
AU  -  Yagishita S
AU  -  Jinde S
AU  -  Kasai K.
PY  - 2026
JO  - PCN Rep
DO  - 10.1002/pcn5.70352
UR  - https://doi.org/10.1002/pcn5.70352
ER  -

APA

A, K., M, T., Y, K., R, M., Y, S., Y, T., S, Y., S, J., & K., K. (2026). Research needs of caregivers of people with 22q11.2 deletion syndrome in Japan: A qualitative analysis.. PCN Rep. https://doi.org/10.1002/pcn5.70352

Source records

europe-pmc · retrieved 2026-09-27T04:23:45.372Z
doaj · retrieved 2026-09-27T04:23:45.379Z