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Publications by Keiko Shimojima
SLC16A2 Mutations in Two Japanese Patients With Allan–Herndon–Dudley Syndrome
Human Genome Variation
Biochemistry
Genetics
Molecular Biology
ACTA2 Is Not a Major Disease-Causing Gene for Moyamoya Disease
Journal of Human Genetics
Genetics
Related publications
Diagnostic and Therapeutic Challenges in the Allan—Herndon—Dudley Syndrome
US Endocrinology
Endocrinology
Metabolism
Diabetes
Two Novel Missense Mutations in the Myostatin Gene Identified in Japanese Patients With Duchenne Muscular Dystrophy
BMC Medical Genetics
Genetics
Novel GRN Mutations in Patients With Corticobasal Syndrome
Scientific Reports
Multidisciplinary
White Matter Abnormalities and Dystonic Motor Disorder Associated With Mutations in the SLC16A2 Gene
Developmental Medicine and Child Neurology
Child Health
Developmental Neuroscience
Pediatrics
Perinatology
Neurology
L-Type Calcium Channel Mutations in Japanese Patients With Inherited Arrhythmias
Circulation Journal
Medicine
Cardiovascular Medicine
Cardiology
Germline Mutations in Japanese Familial Pancreatic Cancer Patients
Oncotarget
Oncology
Mutations in the FGFR2 Gene in Mexican Patients With Apert Syndrome
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
Mutations in the Ribosomal Protein Genes in Japanese Patients With Diamond-Blackfan Anemia
Haematologica
Hematology
Novel USH2A Mutations in Japanese Usher Syndrome Type 2 Patients: Marked Differences in the Mutation Spectrum Between the Japanese and Other Populations
Journal of Human Genetics
Genetics
