Expanding the phenotypic spectrum of NCAPD3-related condensinopathies; a novel variant associated with skeletal anomalies, and autoinflammatory disease

Memiş G., Kalaycı T., Doğru A., Aslanger A. D., Bayrak A. E., Uyguner Z. O.

The European Society of Human Genetics, Milan, Italy, 24 - 27 May 2025, pp.1, (Summary Text)

• Publication Type: Conference Paper / Summary Text
• City: Milan
• Country: Italy
• Page Numbers: pp.1
• Istanbul University Affiliated: Yes