Disease: Amelogenesis imperfecta local hypoplastic form
- A novel AMELX mutation causes hypoplastic amelogenesis imperfecta
- A novel ENAM mutation causes hypoplastic amelogenesis imperfecta
- Defects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfecta
- Dental caries and hypoplastic amelogenesis imperfecta: Clinical, structural, biochemical and molecular approaches
- Distal renal tubular acidosis, autoimmune thyroiditis, enamel hypomaturation, and tooth agenesis caused by homozygosity of a novel double-nucleotide substitution in SLC4A4
- First characterization of LTBP3 variants in two Moroccan families with hypoplastic amelogenesis imperfecta
- Hypoplastic AI with Highly Variable Expressivity Caused by ENAM Mutations
- Hypoplastic amelogenesis imperfecta, bilateral nephrolithiasis and FGF-23-mediated hypophosphataemia: a triad of FAM20A-related enamel renal syndrome
- Hypoplastic amelogenesis imperfecta: Diagnosis approch
- Mineral features of connective dental hard tissues in hypoplastic amelogenesis imperfecta
- Non-syndromic occurrence of true generalized microdontia with hypodontia: A case report
- Novel Ameloblastin Variants, Contrasting Amelogenesis Imperfecta Phenotypes
- Novel CNNM4 variant and clinical features of Jalili syndrome
- Recessive Mutations in ACPT, Encoding Testicular Acid Phosphatase, Cause Hypoplastic Amelogenesis Imperfecta
- SLC13A5 is the second gene associated with Kohlschütter-Tönz syndrome
- Splicing mutations in AMELX and ENAM cause amelogenesis imperfecta
- The implication of holocytochrome c synthase mutation in Korean familial hypoplastic amelogenesis imperfecta