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Publications by Apiruk Sangsin
A Novel De Novo COL1A1 Mutation in a Thai Boy With Osteogenesis Imperfecta Born to Consanguineous Parents
Genetics and Molecular Biology
Genetics
Molecular Biology
Efficacy of Vertebral Cryoablation and Immunotherapy in a Patient With Metastatic Renal Cell Carcinoma: A Case Report
Journal of Medical Case Reports
Medicine
Related publications
A Novel COL1A1 Gene-Splicing Mutation (C.1875+1G>C) in a Brazilian Patient With Osteogenesis Imperfecta
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
Variable Expressivity of Osteogenesis Imperfecta in a Brazilian Family Due to p.G1079S Mutation in the COL1A1 Gene
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
Splice Receptor-Site Mutation C.697-2a>g of the COL1A1 Gene in a Chinese Family With Osteogenesis Imperfecta
Intractable and Rare Diseases Research
Medicine
Correction To: Novel Mutation G324C in WNT1 Mapped in a Large Pakistani Family With Severe Recessively Inherited Osteogenesis Imperfecta
Journal of Biomedical Science
Cell Biology
Pharmacology
Biochemistry
Endocrinology
Clinical Biochemistry
Molecular Biology
Medicine
Metabolism
Diabetes
Structural Models of Osteogenesis Imperfecta-Associated Variants in the COL1A1 Gene
Molecular and Cellular Proteomics
Biochemistry
Medicine
Analytical Chemistry
Molecular Biology
Heterozygous Mutation of C.3521C>T in COL1A1 May Cause Mild Osteogenesis Imperfecta/Ehlers-Danlos Syndrome in a Chinese Family
Intractable and Rare Diseases Research
Medicine
Bilateral Papilledema in a Child With Osteogenesis Imperfecta
Eye and Vision
A Novel De Novo Dominant Mutation inISCUassociated With Mitochondrial Myopathy
Journal of Medical Genetics
Genetics
Osteogenesis Imperfecta
