Nonsense mutations in the hairless gene underlie APL in five families of Pakistani origin
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概要
- 論文の詳細を見る
- 2007-12-01
著者
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Shimomura Yutaka
Department of Dermatology, Niigata University Graduate School of Medicine and Dental Sciences
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Kraemer Liv
Department Of Dermatology Columbia University College Of Physicians And Surgeons
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WAJID Muhammad
Department of Dermatology, Columbia University, College of Physicians and Surgeons
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CHRISTIANO Angela
Department of Dermatology, Columbia University, College of Physicians and Surgeons
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KIM Hyunmi
Department of Dermatology, Columbia University, College of Physicians & Surgeons
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Kim Hyunmi
Department Of Dermatology Columbia University College Of Physicians & Surgeons
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Wajid Muhammad
Department Of Dermatology Columbia University College Of Physicians And Surgeons
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Wajid Muhammad
Department Of Dermatology Columbia University
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Shimomura Yutaka
Department Of Dermatology Columbia University College Of Physicians And Surgeons
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Shimomura Yutaka
Department Of Dermatology Columbia University
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Christiano Angela
Department Of Dermatology Columbia University
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Shimomura Yutaka
Department Of Dermatology College Of Physicians And Surgeons Columbia University
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Christiano Angela
Department Of Dermatology College Of Physicians And Surgeons Columbia University
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Wajid Muhammad
Department Of Dermatology College Of Physicians And Surgeons Columbia University
関連論文
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- Mutations in the desmoglein 1 gene in five Pakistani families with striate palmoplantar keratoderma
- Nonsense mutations in the hairless gene underlie APL in five families of Pakistani origin
- Gene expression of Sh3d19, a novel adaptor protein with five Src homology 3 domains, in anagen mouse hair follicles
- Ambras syndrome in a Korean patient with balanced pericentric inversion (8)(p11.2q24.2)
- Mutations in the LIPH gene in three Japanese families with autosomal recessive woolly hair/hypotrichosis
- Novel compound heterozygous nonsense mutations in the hairless gene causing atrichia with papular lesions
- Striate palmoplantar keratoderma resulting from a frameshift mutation in the desmoglein 1 gene
- A Family of Dynamic Subgrid-Scale Models Consistent with Asymptotic Material Frame Indifference
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- Mutations in the SLURP-1 gene underlie Mal de Meleda in three Pakistani families
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