Ushbu ishga iqtibos qilgan ishlar

2 ta ish

Ish: Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum

1. Loss of Type I Collagen Telopeptide Lysyl Hydroxylation Causes Musculoskeletal Abnormalities in a Zebrafish Model of Bruck Syndrome

   Charlotte Gistelinck, P. Eckhard Witten, Ann Huysseune +12

   MaqolaOAOchiq kirishConnective tissue disorders researchJournal of Bone and Mineral Research20160 iqtibos

   ABIABI:AkademIndex/2016.article.000011

2. Clinical Variability Within the PLOD2-Associated Phenotypic Continuum: Three Novel Variants in Four Patients from a Descriptive Case Series

   Elena S. Merkuryeva, Е. А. Melnik, Vladimir M. Kenis +8

   MaqolaOAOchiq kirishConnective tissue disorders researchGenes20260 iqtibos

   ABIABI:AkademIndex/2026.article.015277