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Publications by Liangzhong Sun
Dent Disease in Chinese Children and Findings From Heterozygous Mothers: Phenotypic Heterogeneity, Fetal Growth, and 10 Novel Mutations
Journal of Pediatrics
Child Health
Pediatrics
Perinatology
The Impact of the COVID-19 Outbreak on the Medical Treatment of Chinese Children With Chronic Kidney Disease (CKD)：A Multicenter Cross-Section Study in the Context of a Public Health Emergency of International Concern
Related publications
Molecular and Phenotypic Abnormalities in Individuals With Germline Heterozygous PTEN Mutations and Autism
Molecular Psychiatry
Psychiatry
Molecular Neuroscience
Mental Health
Molecular Biology
Cellular
Mutation Analysis of 73 Southern Chinese Wilson's Disease Patients: Identification of 10 Novel Mutations and Its Clinical Correlation
Journal of Human Genetics
Genetics
Novel PYGL Mutations in Chinese Children Leading to Glycogen Storage Disease Type VI: Two Case Reports
BMC Medical Genetics
Genetics
Functional and Phenotypic Heterogeneity of Th17 Cells in Health and Disease
European Journal of Clinical Investigation
Medicine
Biochemistry
Clinical Biochemistry
PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity
American Journal of Human Genetics
Genetics
From Lowe Syndrome to Dent Disease: Correlations Between Mutations of the OCRL1 Gene and Clinical and Biochemical Phenotypes
Human Mutation
Genetics
Three Novel Α-L-Iduronidase Mutations in 10 Unrelated Chinese Mucopolysaccharidosis Type I Families
Genetics and Molecular Biology
Genetics
Molecular Biology
Comparison of Clinical Findings Between Lowe Syndrome and Dent Disease With OCRL 1 Mutation
Nihon Shoni Jinzobyo Gakkai Zasshi
Novel Heterozygous Mutations in JAG1 and NOTCH2 Genes in a Neonatal Patient With Alagille Syndrome
Case Reports in Pediatrics
