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Volumn 70, Issue 10, 2008, Pages 744-745

Gap junction protein 12: “Connexing” the pieces in the puzzle of myelination and leukodystrophy

Author keywords

[No Author keywords available]

Indexed keywords

GAP JUNCTION PROTEIN; GJA12 PROTEIN, HUMAN; MEMBRANE PROTEIN; MYELIN PROTEIN; PLP1 PROTEIN, HUMAN; PROTEOLIPID PROTEIN; UNCLASSIFIED DRUG;

EID: 41649114232     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/01.wnl.0000304252.66303.23     Document Type: Editorial
Times cited : (2)

References (10)
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  • 2
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  • 3
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  • 4
    • 0036759150 scopus 로고    scopus 로고
    • Myelin proteolipid protein forms a complex with integrins and may participate in integrin receptor signaling in oligodendrocytes.
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  • 6
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    • Mutations of MLC1 (KIAA0027), encoding a putative membrane protein, cause megalencephalic leukoencephalopathy with subcortical cysts.
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    • Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter.
    • Leegwater PA, Vermeulen G, Konst AA, et al. Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter. Nat Genet 2001;29:383-388.
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    • Leegwater, P.A.1    Vermeulen, G.2    Konst, A.A.3
  • 8
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    • Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease.
    • Uhlenberg B, Schuekle M, Ruschendorf F, et al. Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease. Am J Hum Genet 2004;75:251-260.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.