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Volumn 128 A, Issue 1, 2004, Pages 52-56

Leukoencephalopathy, arthritis, colitis, and hypogammaglobulinemia (LACH) in two brothers: A novel syndrome?

Author keywords

Arthritis; Colitis; Hypogammaglobulinemia; Inflammatory bowel disease; LACH syndrome; Leukoencephalopathy

Indexed keywords

IMMUNOGLOBULIN G1;

EID: 3042724665     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30006     Document Type: Article
Times cited : (2)

References (7)
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  • 4
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    • Update on genetic disorders affecting white matter
    • Kaye EM. 2001. Update on genetic disorders affecting white matter. Pediatr Neurol 24:11-24.
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    • Kaye, E.M.1
  • 5
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    • Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder
    • Nishino I, Spinazzola A, Hirano M. 1999. Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. Science 283:689-692.
    • (1999) Science , vol.283 , pp. 689-692
    • Nishino, I.1    Spinazzola, A.2    Hirano, M.3
  • 7
    • 0034519192 scopus 로고    scopus 로고
    • Congenital disorders of glycosylation: Have you encountered them?
    • Westphal V, Srikrishna G, Freeze HH. 2000. Congenital disorders of glycosylation: have you encountered them? Genet Med 2:329-337.
    • (2000) Genet Med , vol.2 , pp. 329-337
    • Westphal, V.1    Srikrishna, G.2    Freeze, H.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.