Kazuki Kijima

Mitochondrial GTPase mitofusin 2 mutation in Charcot?Marie?Tooth neuropathy type 2A

Kazuki Kijima, Chikahiko Numakura, Hiroko Izumino et al. · Human Genetics · 2004 · 254 citations

Biology, Molecular Neuroscience, Mitochondrial Function +8

Molecular analysis of congenital central hypoventilation syndrome

Ayako Sasaki, Masayo Kanai, Kazuki Kijima et al. · Human Genetics · 2003 · 181 citations

Genetic Disorder, Molecular Analysis, Physiology +2

Cardiac Ion Channel Gene Mutations in Sudden Infant Death Syndrome

Tesshu Otagiri, Kazuki Kijima, Motoki Osawa et al. · Pediatric Research · 2008 · 109 citations · Full text

Cardiac Muscle, Channelopathies, Cardiomyopathy +7

Small heat shock protein 27 mutation in a Japanese patient with distal hereditary motor neuropathy

Kazuki Kijima, Chikahiko Numakura, Tomohide Goto et al. · Journal of Human Genetics · 2005 · 85 citations · Full text

Neurological Disorder, Medicine, Genetics +10

Molecular diagnosis and clinical onset of Charcot–Marie–Tooth disease in Japan

Akiko Abe, Chikahiko Numakura, Kazuki Kijima et al. · Journal of Human Genetics · 2011 · 73 citations · Full text

Clinical Onset, Dental Disease, Pathology