Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2431
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report ; volume:18 ; number:1 ; day:17 ; month:4 ; year:2018 ; pages:1 ; date:12.2018
BMC pediatrics ; 18, Heft 1 (17.4.2018), 1, 12.2018
- Creator
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Lyahyai, Jaber
- Contributor
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Bencheikh, Bouchra Ouled Amar
Elalaoui, Siham C.
Mansouri, Maria
Boualla, Lamia
DIonne-Laporte, Alexandre
Spiegelman, Dan
Dion, Patrick A.
Cossette, Patrick
Rouleau, Guy A.
Sefiani, Abdelaziz
SpringerLink (Online service)
- DOI
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10.1186/s12887-018-1114-y
- URN
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urn:nbn:de:101:1-2018062123343063701929
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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30.01.2005, 4:30 PM CET
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Lyahyai, Jaber
- Bencheikh, Bouchra Ouled Amar
- Elalaoui, Siham C.
- Mansouri, Maria
- Boualla, Lamia
- DIonne-Laporte, Alexandre
- Spiegelman, Dan
- Dion, Patrick A.
- Cossette, Patrick
- Rouleau, Guy A.
- Sefiani, Abdelaziz
- SpringerLink (Online service)
Other Objects (12)
Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report
Pelizaeus-Merzbacher disease (PMD): case report
Pelizaeus Merzbacher disease: dysmyelination versus demyelination
Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease
Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
Generation and characterization of mice expressing a mutation in the connexin47 protein wich causes Pelizaeus-Merzbacher Like Disease in humans
Pelizäus Merzbacher Erkrankung in einem Fall mit Chromosomenanomalie im Bereich des Genorts PLP
Experimentelle Therapie eines Mausmodells für die Pelizaeus-Merzbacher-Erkrankung mit Lonaprisan und Curcumin
Correction to: Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
Merzbacher, Elena geb. Merzbacher
Merzbacher, Elena geb. Merzbacher
Genotype–phenotype correlation and natural history analyses in a Chinese cohort with pelizaeus–merzbacher disease
Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report
Pelizaeus-Merzbacher disease (PMD): case report
Pelizaeus Merzbacher disease: dysmyelination versus demyelination
Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease
Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
Generation and characterization of mice expressing a mutation in the connexin47 protein wich causes Pelizaeus-Merzbacher Like Disease in humans
Pelizäus Merzbacher Erkrankung in einem Fall mit Chromosomenanomalie im Bereich des Genorts PLP
Experimentelle Therapie eines Mausmodells für die Pelizaeus-Merzbacher-Erkrankung mit Lonaprisan und Curcumin
Correction to: Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
Merzbacher, Elena geb. Merzbacher
Merzbacher, Elena geb. Merzbacher
Genotype–phenotype correlation and natural history analyses in a Chinese cohort with pelizaeus–merzbacher disease
Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report
Pelizaeus-Merzbacher disease (PMD): case report
Pelizaeus Merzbacher disease: dysmyelination versus demyelination
Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease
Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
Generation and characterization of mice expressing a mutation in the connexin47 protein wich causes Pelizaeus-Merzbacher Like Disease in humans
Pelizäus Merzbacher Erkrankung in einem Fall mit Chromosomenanomalie im Bereich des Genorts PLP
Experimentelle Therapie eines Mausmodells für die Pelizaeus-Merzbacher-Erkrankung mit Lonaprisan und Curcumin
Correction to: Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
Merzbacher, Elena geb. Merzbacher
Merzbacher, Elena geb. Merzbacher