TRAPPC2

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Authors: baitao zeng
Cited by: 0

Abstract

Identification of a novel deletion variant in TRAPPC2 in a Chinese family with X-linked spondyloepiphyseal dysplasia tarda

Fields of Study & Subjects

Connective tissue disorders research Genomics and Rare Diseases Osteoarthritis Treatment and Mechanisms

Publication details

Journal / source
Figshare
Publication date
1 January 2026
Document type
Dataset