Expanding the phenotypic spectrum of PROK2/PROKR2: a recall-by-genotype study
Year: 2025
Type: article
Study design: Observational Study
Source: Human Genetics
Institutions: Harvard University, Massachusetts General Hospital
Language: English
Subfield: Reproductive Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: green
Funders: National Institutes of Health, U.S. Food and Drug Administration, National Institute of Child Health and Human Development, National Institute of Dental and Craniofacial Research, National Center for Advancing Translational Sciences, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: The Harvard Clinical and Translational Science Center, G3150096190, Deciphering the Role of Copy Number Variants in Neuroendocrine Disorders of Infertility, Integrative Approaches to Decipher Genetic Determinants of Disease Penetrance in Prokineticin 2 Pathway Related Human Reproductive Disorders, Harvard Clinical and Translational Science Center, Towards Curative Therapies for Hypogonadotropic Diseases, The Massachusetts General Hospital Harvard Center for Reproductive Medicine, Elucidating the Role of the FGFR1 Signaling Pathway in the Intersection of Reproduction and Metabolism, Dissection of the Molecular Basis of Pleiotropy Between GnRH Neuronal Development and Cranial Suture Fusion
OpenAlex ID: W4411213167