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[Pelizaeus-Merzbacher-caused diseases in Connexin 46 mutation: a rare form of leukodystrophy].

RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin - 1 Jun 2007

Fritz G A, Simbrunner J, Deutschmann H A

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Identifiers

PMID: 17492548
DOI: 10.1055/s-2007-963009

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[Pelizaeus-Merzbacher-caused diseases in Connexin 46 mutation: a rare form of leukodystrophy].PMID 17492548Read ↗

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A cellular mechanism governing the severity of Pelizaeus-Merzbacher disease.Semantic proximity Read ↗

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Diseases of connexins expressed in myelinating glia.Semantic proximity Read ↗

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