Работы, цитирующие эту работу

Работ: 2

Работа: Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen

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

   СтатьяConnective tissue disorders researchJournal of Bone and Mineral Research2016Цитирований: 0

   ABIABI:AkademIndex/openalex/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

   СтатьяConnective tissue disorders researchGenes2026Цитирований: 0

   ABIABI:AkademIndex/openalex/2026.article.015277