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Volumn 133, Issue 6, 2013, Pages 1688-1690

Late-onset X-linked dominant protoporphyria: An etiology of photosensitivity in the elderly

Author keywords

[No Author keywords available]

Indexed keywords

PERINDOPRIL; PORPHYRIN;

EID: 84878559551     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/jid.2012.467     Document Type: Letter
Times cited : (14)

References (11)
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  • 2
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  • 3
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    • Acquired erythropoietic protoporphyria
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    • Blagojevic, D.1    Schenk, T.2    Haas, O.3
  • 4
    • 79958726106 scopus 로고    scopus 로고
    • Characteristics and outcome of myelodysplastic syndromes (MDS) with isolated 20q deletion: A report on 62 cases
    • Braun T, de Botton S, Taksin AL et al. (2011) Characteristics and outcome of myelodysplastic syndromes (MDS) with isolated 20q deletion: a report on 62 cases. Leuk Res 35:863-7
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  • 5
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  • 6
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    • Ge B, Gurd S, Gaudin T et al. (2005) Survey of allelic expression using EST mining. Genome Res 15:1584-91
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    • Ge, B.1    Gurd, S.2    Gaudin, T.3
  • 7
    • 20244389965 scopus 로고    scopus 로고
    • Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS)
    • Gibbons RJ, Pellagatti A, Garrick D et al. (2003) Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS). Nat Genet 34:446-9
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  • 8
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    • Contribution of a common singlenucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyria
    • Gouya L, Martin-Schmitt C, Robreau AM et al. (2006) Contribution of a common singlenucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyria. Am J Hum Genet 78:2-14
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    • Gouya, L.1    Martin-Schmitt, C.2    Robreau, A.M.3
  • 10
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    • The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: Rationale and important changes
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  • 11
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    • C-terminal deletions in the ALAS2 gene lead to gain of function and cause X-linked dominant protoporphyria without anemia or iron overload
    • Whatley SD, Ducamp S, Gouya L et al. (2008) C-terminal deletions in the ALAS2 gene lead to gain of function and cause X-linked dominant protoporphyria without anemia or iron overload. Am J Hum Genet 83:408-14
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    • Whatley, S.D.1    Ducamp, S.2    Gouya, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.