Associated Papers
Perspectives on the implications of carrying putative pathogenic variants in the medulloblastoma predisposition genes ELP1 and GPR161.
Smith MJ et al.
Familial Cancer, 2023
Dominant negative GPR161 rare variants are risk factors of human spina bifida.
Kim SE et al.
Human Molecular Genetics, 2019
Whole-exome sequencing identifies homozygous GPR161 mutation in a family with pituitary stalk interruption syndrome.
Karaca E et al.
The Journal of Clinical Endocrinology and Metabolism, 2015
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