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Details on Person Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene
| Class:Id | LiteratureReference:3656483 |
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| _displayName | Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene |
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| _timestamp | 2013-06-05 15:32:16 |
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| author | [Person:3656459] Akama, T O
[Person:2534119] Nishida, K
[Person:3656422] Nakayama, J
[Person:2426488] Watanabe, H
[Person:3656460] Ozaki, K
[Person:2327721] Nakamura, T
[Person:3656416] Dota, A
[Person:3656425] Kawasaki, S
[Person:3656431] Inoue, Y
[Person:3656424] Maeda, N
[Person:3223204] Yamamoto, S
[Person:3656462] Fujiwara, Toshiyuki
[Person:3656476] Thonar, E J
[Person:3656482] Shimomura, Y
[Person:2534120] Kinoshita, S
[Person:3656463] Tanigami, A
[Person:3656479] Fukuda, M N |
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| created | [InstanceEdit:3656412] Jassal, B, 2013-06-05 |
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| journal | Nat. Genet. |
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| pages | 237-41 |
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| pubMedIdentifier | 11017086 |
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| title | Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene |
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| volume | 26 |
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| year | 2000 |
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| (literatureReference) | [FailedReaction:3656269] Defective CHST6 does not transfer SO4(2-) to GlcNAc residues on keratan-PG [Homo sapiens] |
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