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Author/Creator Nakayama, Atsuo

2. Identification of novel compound heterozygous mutations in ACO2 in a patient with progressive cerebral and cerebellar atrophy. Issue 7 (20th May 2019)

Authors:
Fukada, Masahide; Yamada, Keitaro; Eda, Shima; Inoue, Ken; Ohba, Chihiro; Matsumoto, Naomichi; Saitsu, Hirotomo; Nakayama, Atsuo
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 7(2019)
Page Start:
n/a
Record Type:
Journal Article
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4. Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4. (11th December 2013)

Authors:
Kimura, Masashi; Machida, Junichiro; Yamaguchi, Seishi; Shibata, Akio; Tatematsu, Tadashi; Miyachi, Hitoshi; Jezewski, Peter A.; Nakayama, Atsuo; Higashi, Yujiro; Shimozato, Kazuo; Tokita, Yoshihito
Journal:
European journal of oral sciences
Issue:
Volume 122:Number 1(2014:Feb.)
Page Start:
15
Record Type:
Journal Article
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5. Novel RUNX2/CBFA1 mutation in the runt domain in a Japanese patient with cleidocranial dysplasia. Issue 3 (May 2017)

Authors:
Goto, Hiroki; Machida, Junichiro; Shibata, Akio; Tatematsu, Tadashi; Osumi, Eriko; Miyachi, Hitoshi; Takahashi, Katsu; Nakayama, Atsuo; Higashi, Yujiro; Nagao, Toru; Shimozato, Kazuo; Tokita, Yoshihito
Journal:
Journal of oral and maxillofacial surgery, medicine, and pathology
Issue:
Volume 29:Issue 3(2017)
Page Start:
222
Record Type:
Journal Article
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