Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Fatih Ozaltin

Mutations in KEOPS-complex Genes Cause Nephrotic Syndrome With Primary Microcephaly

Nature Genetics

English

MYO1EMutations and Childhood Familial Focal Segmental Glomerulosclerosis

New England Journal of Medicine

English

Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome

American Journal of Human Genetics

English

Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype With ESRD

Journal of the American Society of Nephrology : JASN

English

Normal 25-Hydroxyvitamin D Levels Are Associated With Less Proteinuria and Attenuate Renal Failure Progression in Children With CKD

Journal of the American Society of Nephrology : JASN

English

The Clinical and Mutational Spectrum of Turkish Patients With Cystinosis

Clinical Journal of the American Society of Nephrology

Transplantation

Intensive Care Medicine

English

Respiratory-Chain Deficiency Presenting as Diffuse Mesangial Sclerosis With NPHS3 Mutation

Pediatric Nephrology

English