Van Maldergem Syndrome-1 with Central Precocious Puberty: Expanding the Clinical and Genetic Spectrum
Year: 2025
Type: article
Abstract: Van Maldergem syndrome-1 (VMS-1) is an ultrarare autosomal recessive disorder caused by pathogenic variants in DCHS1
Author: Bo Xu
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: diamond
OpenAlex ID: W4414864236
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