Associated Papers
Simultaneous CNV-seq and WES: An effective strategy for molecular diagnosis of unexplained fetal structural anomalies.
Zhang H et al.
Heliyon, 2024
Mutations in CSPP1, encoding a core centrosomal protein, cause a range of ciliopathy phenotypes in humans.
Shaheen R et al.
American Journal of Human Genetics, 2014
Mutations in CSPP1 lead to classical Joubert syndrome.
Akizu N et al.
American Journal of Human Genetics, 2014
Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy.
Tuz K et al.
American Journal of Human Genetics, 2014
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