Occurrence of Emery-Dreifuss muscular dystrophy in a rural setting of Cameroon: a case report and review of the literature
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1756-0500
- 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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Occurrence of Emery-Dreifuss muscular dystrophy in a rural setting of Cameroon: a case report and review of the literature ; volume:10 ; number:1 ; day:9 ; month:1 ; year:2017 ; pages:1-5 ; date:12.2017
BMC Research Notes / Biomed Central; 10, Heft 1 (9.1.2017), 1-5, 12.2017
- Keyword
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Orthopädie
- Creator
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Ekabe, Cyril Jabea
- Contributor
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Kehbila, Jules
Sama, Carlson–Babila
Kadia, Benjamin Momo
Abanda, Martin Hongieh
Monekosso, Gottlieb Lobe
SpringerLink (Online service)
- DOI
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10.1186/s13104-016-2363-1
- URN
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urn:nbn:de:1111-201702087365
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 11:00 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Ekabe, Cyril Jabea
- Kehbila, Jules
- Sama, Carlson–Babila
- Kadia, Benjamin Momo
- Abanda, Martin Hongieh
- Monekosso, Gottlieb Lobe
- SpringerLink (Online service)
Other Objects (12)
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Perinatal Management of Pregnancy Complicated by Autosomal Dominant Emery–Dreifuss Muscular Dystrophy
Isolated Right Atrial Enhancement with Atrial Standstill: An Uncommon Presentation of Emery–Dreifuss Muscular Dystrophy
A novel SYNE1 gene mutation in a Chinese family of Emery-Dreifuss muscular dystrophy-like
Impairment of Lamin A/C-Polycomb crosstalk as a possible epigenetic cause of Emery Dreifuss Muscular Dystrophy (EDMD)
Lamin A and lamin C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy
In vitro contracture test results and anaesthetic management of a patient with emery-dreifuss muscular dystrophy for cardiac transplantation
Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery–Dreifuss muscular dystrophy caused by an LMNA gene mutation
Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case report
Mutationsanalyse von Kandidatengenen für die Emery-Dreifuss Muskeldystrophie in der Region Xq 28
Lengyel, Emery
FHL1 protein isoforms in Emery-Dreifuss muscular dystrophy
Advances in muscle imaging for Emery-Dreifuss muscular dystrophy
Perinatal Management of Pregnancy Complicated by Autosomal Dominant Emery–Dreifuss Muscular Dystrophy
Isolated Right Atrial Enhancement with Atrial Standstill: An Uncommon Presentation of Emery–Dreifuss Muscular Dystrophy
A novel SYNE1 gene mutation in a Chinese family of Emery-Dreifuss muscular dystrophy-like
Impairment of Lamin A/C-Polycomb crosstalk as a possible epigenetic cause of Emery Dreifuss Muscular Dystrophy (EDMD)
Lamin A and lamin C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy
In vitro contracture test results and anaesthetic management of a patient with emery-dreifuss muscular dystrophy for cardiac transplantation
Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery–Dreifuss muscular dystrophy caused by an LMNA gene mutation
Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case report
Mutationsanalyse von Kandidatengenen für die Emery-Dreifuss Muskeldystrophie in der Region Xq 28
Lengyel, Emery
FHL1 protein isoforms in Emery-Dreifuss muscular dystrophy
Advances in muscle imaging for Emery-Dreifuss muscular dystrophy
Perinatal Management of Pregnancy Complicated by Autosomal Dominant Emery–Dreifuss Muscular Dystrophy
Isolated Right Atrial Enhancement with Atrial Standstill: An Uncommon Presentation of Emery–Dreifuss Muscular Dystrophy
A novel SYNE1 gene mutation in a Chinese family of Emery-Dreifuss muscular dystrophy-like
Impairment of Lamin A/C-Polycomb crosstalk as a possible epigenetic cause of Emery Dreifuss Muscular Dystrophy (EDMD)
Lamin A and lamin C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy
In vitro contracture test results and anaesthetic management of a patient with emery-dreifuss muscular dystrophy for cardiac transplantation
Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery–Dreifuss muscular dystrophy caused by an LMNA gene mutation
Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case report
Mutationsanalyse von Kandidatengenen für die Emery-Dreifuss Muskeldystrophie in der Region Xq 28