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Publications by Masahide Ikema
A Founder Mutation of CANT1 Common in Korean and Japanese Desbuquois Dysplasia
Journal of Human Genetics
Genetics
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CANT1 Deficiency in a Mouse Model of Desbuquois Dysplasia Impairs Glycosaminoglycan Synthesis and Chondrocyte Differentiation in Growth Plate Cartilage
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A Common Founder Mutation in the EDA-A1 Gene in X-Linked Hypodontia
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A Common Founder for the 35delG GJB2 Gene Mutation in Connexin 26 Hearing Impairment
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Analysis of Clinical Characteristics of Breast Cancer Patients With the Japanese Founder Mutation BRCA1 L63X
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A Founder Mutation in CERKL Is a Major Cause of Retinal Dystrophy in Finland
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HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1−/− Mice
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Autosomal Dominant Nocturnal Frontal Lobe Epilepsy: A Genotypic Comparative Study of Japanese and Korean Families Carrying the CHRNA4 Ser284Leu Mutation
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Phenotypic Heterogeneity in British Patients With a Founder Mutation in the FHL1 Gene
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