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Two children with hypophosphatasia with a heterozygous c.1559delT variant in the ALPL gene, the most common variant in Japanese populations.
Kitoh, Hiroshi; Izawa, Masako; Kaneko, Hiroshi; Kitamura, Akiko; Matsuyama, Saori; Kato, Kohji; Ogi, Tomoo.
Affiliation
  • Kitoh H; Department of Orthopaedic Surgery, Aichi Children's Health and Medical Center, 7-426 Morioka-cho, Obu, Aichi 474-8710, Japan.
  • Izawa M; Department of Comprehensive Pediatric Medicine, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi 466-8550, Japan.
  • Kaneko H; Department of Endocrinology and Metabolism, Aichi Children's Health and Medical Center, 7-426 Morioka-cho, Obu, Aichi 474-8710, Japan.
  • Kitamura A; Department of Orthopaedic Surgery, Aichi Children's Health and Medical Center, 7-426 Morioka-cho, Obu, Aichi 474-8710, Japan.
  • Matsuyama S; Department of Orthopaedic Surgery, Aichi Children's Health and Medical Center, 7-426 Morioka-cho, Obu, Aichi 474-8710, Japan.
  • Kato K; Department of Orthopaedic Surgery, Aichi Children's Health and Medical Center, 7-426 Morioka-cho, Obu, Aichi 474-8710, Japan.
  • Ogi T; Department of Genetics, Research Institute of Environmental Medicine (RIeM), Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Aichi 464-8601, Japan.
Bone Rep ; 17: 101626, 2022 Dec.
Article in En | MEDLINE | ID: mdl-36217348
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Bone Rep Year: 2022 Document type: Article Affiliation country:
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Bone Rep Year: 2022 Document type: Article Affiliation country: