RAB33B and PCNT variants in two Pakistani families with skeletal dysplasia and short stature

Skeletal dysplasia is a heterogeneous group of disorders resulting from different genetic variants in humans. The current study was designed to identify the genetic causes of skeletal dysplasia and short statu...

Source: BMC Musculoskeletal Disorders - July 20, 2021 Category: Orthopaedics Authors: Noor ul Ain, Zunaira Fatima, Sadaf Naz and Outi Makitie Tags: Research Source Type: research