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Publications by Sol Kang
A Case of Autosomal Dominant Osteopetrosis Type II With a CLCN7 Gene Mutation
JCRPE Journal of Clinical Research in Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Related publications
A Patient With a Novel Gene Mutation Leading to Autosomal Dominant Polycystic Kidney Disease
Clinical Journal of the American Society of Nephrology
Epidemiology
Nephrology
Critical Care
Transplantation
Intensive Care Medicine
a Novel HSF4 Gene Mutation Causes Autosomal-Dominant Cataracts in a Chinese Family
G3: Genes, Genomes, Genetics
Medicine
Genetics
Molecular Biology
A Novel Dominant Mutation in the SOX10 Gene in a Chinese Family With Waardenburg Syndrome Type�II
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Dystonia in a Patient With Autosomal-Dominant Progressive External Ophthalmoplegia Type 1 Caused by Mutation in the POLG Gene
Movement Disorders Clinical Practice
Neurology
Genotyping, Generation and Proteomic Profiling of the First Human Autosomal Dominant Osteopetrosis Type II-specific Induced Pluripotent Stem Cells
Stem Cell Research and Therapy
Genetics
Cell Biology
Molecular Biology
Biochemistry
Medicine
Molecular Medicine
A Novel Mutation in the Connexin 46 Gene Causes Autosomal Dominant Congenital Cataract With Incomplete Penetrance
Journal of Medical Genetics
Genetics
A Novel FBN1 Mutation Causes Autosomal Dominant Marfan Syndrome
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy in a Spanish Family With a Ser252Phe Mutation in the CHRNA4 Gene
Archives of Neurology
Autosomal Dominant Macular Degeneration Associated With 208del G Mutation in the FSCN2 Gene
Archives of Ophthalmology
