Cockayne syndrome type A : novel mutations in eight typical patients
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概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2006-08-01
著者
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Kim Chong
Genetic Unit Department Of Pediatrics University Of Sao Paulo Medical School
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CAO Henian
Robarts Research Institute, University of Western Ontario
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Hegele Robert
Robarts Research Institute
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Cao Henian
Robarts Research Institute
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BERTOLA Debora
Genetics Clinic Unit, Instituto da Crianca do Hospital das Clinicas, University of Sao Paulo
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ALBANO Lilian
Genetics Clinic Unit, Instituto da Crianca do Hospital das Clinicas, University of Sao Paulo
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OLIVEIRA Daniela
Department of Neurology, University of Sao Paulo
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KOK Fernando
Department of Neurology, University of Sao Paulo
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MARQUES-DIAS Maria
Department of Neurology, University of Sao Paulo
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Marques-dias Maria
Department Of Neurology University Of Sao Paulo
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Albano Lilian
Genetics Clinic Unit Instituto Da Crianca Do Hospital Das Clinicas University Of Sao Paulo
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Bertola Debora
Genetics Clinic Unit Instituto Da Crianca Do Hospital Das Clinicas University Of Sao Paulo
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Kok Fernando
Department Of Neurology University Of Sao Paulo
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Kok Fernando
Departamento De Neurologia Do Hospital Das Clinicas Da Faculdade De Medicina Da Universidade De Sao
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Oliveira Daniela
Department Of Neurology University Of Sao Paulo
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Kim Chong
Genetics Clinic Unit Instituto Da Crianca Do Hospital Das Clinicas University Of Sao Paulo
関連論文
- Identification of single-nucleotide polymorphisms in the human LPIN1 gene
- Cockayne syndrome type A : novel mutations in eight typical patients
- CKN1 (MIM 216400) : mutations in Cockayne syndrome type A and a new common polymorphism
- A study of EEG and epilepsy profile in Wolf-Hirschhorn syndrome and considerations regarding its correlation with other chromosomal disorders
- Pediatric multiple sclerosis report of 14 cases
- Identification of novel L2HGDH gene mutations and update of the pathological spectrum