Case Report: A Novel Homozygous Missense Variant of FBN3 Supporting It Is a New Candidate Gene Causative of a Bardet–Biedl Syndrome–Like Phenotype

Overview of attention for article published in Frontiers in Genetics, July 2022

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Case Report: A Novel Homozygous Missense Variant of FBN3 Supporting It Is a New Candidate Gene Causative of a Barde… https://t.co/rhULkGTi9U

02 Aug 2022

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New Research: Case Report: A Novel Homozygous Missense Variant of FBN3 Supporting It Is a New Candidate Gene Causative of a Bardet–Biedl Syndrome–Like Phenotype: Fibrillin proteins are extracellular matrix glycoproteins assembling into… https://t.co/bCcHX1

15 Jul 2022

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