학술논문
Case Report: A Novel Homozygous Missense Variant of FBN3 Supporting It Is a New Candidate Gene Causative of a Bardet–Biedl Syndrome–Like Phenotype
Document Type
Article
Author
Source
In: Frontiers in Genetics . (Frontiers in Genetics, 15 July 2022, 13)
Subject
Language
English
ISSN
16648021