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mps2-database index page

The purpose of this database is to support researchers and clinicians. Understand structural changes on IDS caused by MPSII mutation. This database contains clinical phenotypes, genotypes, and structures of mutant IDSs. It is freely accessible and can be reproduced if proper reference is made to the database and its contributions. This database was constructed and maintained by the research group lead by. HSakuraba( department of clinical genetics. Last updated 2016/05/23 ver.0.1.0).

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The purpose of this database is to support researchers and clinicians. Understand structural changes on IDS caused by MPSII mutation. This database contains clinical phenotypes, genotypes, and structures of mutant IDSs. It is freely accessible and can be reproduced if proper reference is made to the database and its contributions. This database was constructed and maintained by the research group lead by. HSakuraba( department of clinical genetics. Last updated 2016/05/23 ver.0.1.0).
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mps2-database index page | mps2-database.org Reviews

https://mps2-database.org

The purpose of this database is to support researchers and clinicians. Understand structural changes on IDS caused by MPSII mutation. This database contains clinical phenotypes, genotypes, and structures of mutant IDSs. It is freely accessible and can be reproduced if proper reference is made to the database and its contributions. This database was constructed and maintained by the research group lead by. HSakuraba( department of clinical genetics. Last updated 2016/05/23 ver.0.1.0).

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my-pharm.ac.jp my-pharm.ac.jp

明治薬科大学 | 臨床遺伝学講座

http://www.my-pharm.ac.jp/genetics

臨床遺伝学公開シンポジウム2016 リソソーム病 基礎から研究へ を開催しました。 ムコ多糖症 型データベース http:/ mps2-database.org/ を公開しました。 臨床遺伝学公開シンポジウム2015 リソソーム病 現在と未来 を開催しました。 ムコ多糖症 型データベース http:/ mps1-database.org/ を公開しました。 ファブリー病データベース http:/ fabry-database.org/ を更新しました。 臨床遺伝学講座 寄附講座 が、分析化学教室と共同で3月10日に臨床遺伝学公開シンポジウム2012 リソソーム病研究 さらなる進歩に向って を開催しました。 ムコ多糖症 型のデータベース http:/ mps6-database.org を公開しました。 ファブリー病データベース http:/ fabry-database.org を更新しました。 本講座では、遺伝性難病、特に リソソーム ライソゾーム 病 と呼ばれる病気の病態解明と診断 治療法の開発を目指した研究を行っています。 TEL and FAX 042-495-8923.

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mps2-database index page

The purpose of this database is to support researchers and clinicians. Understand structural changes on IDS caused by MPSII mutation. This database contains clinical phenotypes, genotypes, and structures of mutant IDSs. It is freely accessible and can be reproduced if proper reference is made to the database and its contributions. This database was constructed and maintained by the research group lead by. HSakuraba( department of clinical genetics. Last updated 2016/05/23 ver.0.1.0).

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