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Publications by Tetsuo Hattori

Two Novel Mutations of the CYP11B2 Gene in a Japanese Patient With Aldosterone Deficiency Type 1

Endocrine Journal

English

Related publications

A Novel Nonsense Mutation of the PEPD Gene in a Japanese Patient With Prolidase Deficiency

Journal of Human Genetics

English

Two Novel Mutations in the SLC25A4 Gene in a Patient With Mitochondrial Myopathy

Internal Medicine

Molecular Biology

English

Three Novel Mutations in the Glycoprotein IIb Gene in a Patient With Type II Glanzmann Thrombasthenia

English

Two Unrelated Patients With Rare Crigler-Najjar Syndrome Type I: Two Novel Mutations and a Patient With Loss of Heterozygosity of UGT1A1 Gene

Journal of Zhejiang University: Science B

Molecular Biology

English

Two Novel Missense Mutations in the Myostatin Gene Identified in Japanese Patients With Duchenne Muscular Dystrophy

BMC Medical Genetics

English

Congenital Dyserythropoietic Anemia Type 1: A Case With Novel Compound Heterozygous Mutations in the C15orf41 Gene

American Journal of Hematology

English

Novel MEN1 Gene Mutations in Familial Multiple Endocrine Neoplasia Type 1

Journal of Human Genetics

English

Three Novel Mutations of the PAX6 Gene in Japanese Aniridia Patients

Journal of Human Genetics

English

A Novel Compound Heterozygous Mutation of the AIRE Gene in a Patient With Autoimmune Polyendocrine Syndrome Type 1

Annals of Pediatric Endocrinology and Metabolism

English