Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort study. (2023)
Attributed to:
Early Life Aetiology and Mechanisms of Diabetes and Related Metabolic Disorders
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/s2213-8587(23)00131-6
PubMed Identifier: 37385287
Publication URI: http://europepmc.org/abstract/MED/37385287
Type: Journal Article/Review
Volume: 11
Parent Publication: The lancet. Diabetes & endocrinology
Issue: 8
ISSN: 2213-8587