Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy
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Journal
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- Journal of human genetics / Japan Society of Human Genetics
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Journal of human genetics / Japan Society of Human Genetics 59 (8), 444-453, 2014-08
Tokyo : Springer Nature
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Details 詳細情報について
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- CRID
- 1520010380347222144
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- NII Article ID
- 40020171705
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- NII Book ID
- AA11206160
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- ISSN
- 14345161
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- NDL BIB ID
- 025732070
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- Text Lang
- en
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- NDL Source Classification
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- ZS16(科学技術--医学--人類遺伝学)
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- Data Source
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- NDL
- CiNii Articles
