Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutation

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1756-6606

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutation ; volume:10 ; number:1 ; day:13 ; month:4 ; year:2017 ; pages:1-13 ; date:12.2017
Molecular brain ; 10, Heft 1 (13.4.2017), 1-13, 12.2017

Keyword: Hirnkrankheit
Neuropsychiatrie
Nervenkrankheit

Creator: Choquet, Karine

Contributor: Yang, Sharon
Moir, Robyn D.
Forget, Diane
Larivière, Roxanne
Bouchard, Annie
Poitras, Christian
Sgarioto, Nicolas
Dicaire, Marie-Josée
Noohi, Forough
Kennedy, Timothy E.
Rochford, Joseph
Bernard, Geneviève
Teichmann, Martin
Coulombe, Benoit
Willis, Ian M.
Kleinman, Claudia L.
Brais, Bernard
SpringerLink (Online service)

DOI: 10.1186/s13041-017-0294-y

URN: urn:nbn:de:1111-201704302795

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:46 AM CEST

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Associated

Choquet, Karine
Yang, Sharon
Moir, Robyn D.
Forget, Diane
Larivière, Roxanne
Bouchard, Annie
Poitras, Christian
Sgarioto, Nicolas
Dicaire, Marie-Josée
Noohi, Forough
Kennedy, Timothy E.
Rochford, Joseph
Bernard, Geneviève
Teichmann, Martin
Coulombe, Benoit
Willis, Ian M.
Kleinman, Claudia L.
Brais, Bernard
SpringerLink (Online service)

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Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutation

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Other Objects (12)

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Isolated proteinuria due to CUBN homozygous mutation – challenging the investigative paradigm

Tocilizumab reverses cerebral vasculopathy in a patient with homozygous SAMHD1 mutation

A rare homozygous missense mutation of COL7A1 in a Vietnamese family

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A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy

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Isolated proteinuria due to CUBN homozygous mutation – challenging the investigative paradigm

Tocilizumab reverses cerebral vasculopathy in a patient with homozygous SAMHD1 mutation

A rare homozygous missense mutation of COL7A1 in a Vietnamese family

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