A Novel Deletion Mutation in Proteoglycan-4 Underlies Camptodactyly-Arthropathy-Coxa-Vara-Pericarditis Syndrome in a Consanguineous Pakistani Family
Sulman Basit, Zafar Iqbal, Masha Umicevic-Mirkov, Syed Kamran Ul-Hassan Naqvi, Marieke Coenen, Muhammad Ansar, Hans van Bokhoven, Wasim AhmadVolume:
42
Year:
2011
Language:
english
Pages:
5
DOI:
10.1016/j.arcmed.2011.04.006
File:
PDF, 514 KB
english, 2011