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Publications by Sumeda Nandadasa

Mutations of ADAMTS9 Cause Nephronophthisis-Related Ciliopathy

American Journal of Human Genetics
Genetics
2019English

Related publications

Mutations of CEP83 Cause Infantile Nephronophthisis and Intellectual Disability

American Journal of Human Genetics
Genetics
2014English

Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype With ESRD

Journal of the American Society of Nephrology : JASN
MedicineNephrology
2014English

Mutations of IFT81, Encoding an IFT-B Core Protein, as a Rare Cause of a Ciliopathy

Cilia
Cell Biology
2015English

Bi-Allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans

American Journal of Human Genetics
Genetics
2019English

Nephronophthisis

European Journal of Human Genetics
Genetics
2008English

Nephronophthisis

Pediatric Nephrology
Child HealthPediatricsPerinatologyNephrology
2008English

Mainzer-Saldino Syndrome Is a Ciliopathy Caused by Mutations in the IFT140 Gene

Cilia
Cell Biology
2012English

ACTN1 Mutations Cause Congenital Macrothrombocytopenia

American Journal of Human Genetics
Genetics
2013English

LRIG2 Mutations Cause Urofacial Syndrome

American Journal of Human Genetics
Genetics
2013English

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