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Publications by Peter Kannu

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

Nature Genetics

English

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Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome

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Human Mutations in NDE1 Cause Extreme Microcephaly With Lissencephaly

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Mutations in KIRREL1, a Slit Diaphragm Component, Cause Steroid-Resistant Nephrotic Syndrome

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An Unusual Cause for Nephrotic Syndrome: Nephrotic Syndrome Due to Metformin

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Barth Syndrome Mutations That Cause Tafazzin Complex Lability

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Inactivating Mutations in MFSD2A, Required for Omega-3 Fatty Acid Transport in Brain, Cause a Lethal Microcephaly Syndrome

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Primary Microcephaly-Epilepsy-Permanent Neonatal Diabetes Syndrome

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Two Novel NPHS1 Mutations in a Chinese Family With Congenital Nephrotic Syndrome

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Histopathological Features of Primary Nephrotic Syndrome in Children

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