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Publications by Peiran Zhou

Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients

PLoS ONE
Multidisciplinary
2014English

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Novel Mutations in COL4A3, COL4A4, and COL4A5 in Chinese Patients With Alport Syndrome

PLoS ONE
Multidisciplinary
2017English

Bruck Syndrome

2020English

Novel GRN Mutations in Patients With Corticobasal Syndrome

Scientific Reports
Multidisciplinary
2016English

Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome

American Journal of Human Genetics
Genetics
2019English

Twelve Novel Atm Mutations Identified in Chinese Ataxia Telangiectasia Patients

NeuroMolecular Medicine
Molecular NeuroscienceNeurologyMolecular MedicineCellular
2013English

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

Genetics and Molecular Research
MedicineGeneticsMolecular Biology
2011English

Novel IRF6 Mutations in Honduran Van Der Woude Syndrome Patients

Molecular Medicine Reports
OncologyGeneticsMolecular BiologyBiochemistryCancer ResearchMolecular Medicine
2011English

LRIG2 Mutations Cause Urofacial Syndrome

American Journal of Human Genetics
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2013English

Novel NPHS1 Splice Site Mutations in a Chinese Child With Congenital Nephrotic Syndrome

Genetics and Molecular Research
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2015English

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