A case of bipolar I disorder with a loss-of-function variant of schizophrenia risk gene SETD1A: possible expansion of the relevant clinical spectrum supported by a meta-analysis
Psychiatry Clin Neurosci
.
2024 Apr 22.
doi: 10.1111/pcn.13669.
Online ahead of print.
Authors
Tomonori Hara
1
2
3
,
An-A Kazuno
1
,
Tomoko Toyota
1
4
,
Junko Ueda
1
,
Takehiko Shuno
5
,
Jun Mukai
6
,
Taka-Aki Sato
6
,
Naomichi Matsumoto
7
,
Takeo Yoshikawa
8
,
Atsushi Takata
1
9
Affiliations
1
Laboratory for Molecular Pathology of Psychiatric Disorders, RIKEN Center for Brain Science, Wako, Japan.
2
Department of Organ Anatomy, Tohoku University Graduate School of Medicine, Sendai, Japan.
3
Hatsuishi Hospital, Kashiwa, Japan.
4
Kokoro Medical Office, Akita, Japan.
5
Asai Hospital, Togane, Japan.
6
Research and Development Center for Precision Medicine, University of Tsukuba, Tsukuba, Japan.
7
Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
8
Laboratory for Molecular Psychiatry, RIKEN Center for Brain Science, Wako, Japan.
9
Research Institute for Diseases of Old Age, Juntendo University Graduate School of Medicine, Bunkyo-Ku, Japan.
PMID:
38646907
DOI:
10.1111/pcn.13669
No abstract available
Publication types
Letter
Grants and funding
JP20dm0107133/Japan Agency for Medical Research and Development
JP20dm0307028/Japan Agency for Medical Research and Development
JP22km0405214/Japan Agency for Medical Research and Development
JP23ek0109549/Japan Agency for Medical Research and Development
JP23ek0109617/Japan Agency for Medical Research and Development
JP23ek0109674/Japan Agency for Medical Research and Development
JP20H05777/Japan Society for the Promotion of Science
JP21H02855/Japan Society for the Promotion of Science