A novel mutation in ITGB4 gene in a newborn with epidermolysis bullosa, pyloric atresia, and aplasia cutis congenita
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2090-2441
- 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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A novel mutation in ITGB4 gene in a newborn with epidermolysis bullosa, pyloric atresia, and aplasia cutis congenita ; volume:21 ; number:1 ; day:1 ; month:4 ; year:2020 ; pages:1-4 ; date:12.2020
The Egyptian journal of medical human genetics ; 21, Heft 1 (1.4.2020), 1-4, 12.2020
- Creator
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Okulu, Emel
Durmaz, Ceren D.
Tunc, Gaffari
Guzel, Adil
Kutlay, Nuket Y.
Erdeve, Omer
Atasay, Begum
McGrath, John A.
Liu, Lu
Arsan, Saadet
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s43042-020-00055-7
- URN
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urn:nbn:de:101:1-2020062500032473336677
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:44 AM CEST
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
- Okulu, Emel
- Durmaz, Ceren D.
- Tunc, Gaffari
- Guzel, Adil
- Kutlay, Nuket Y.
- Erdeve, Omer
- Atasay, Begum
- McGrath, John A.
- Liu, Lu
- Arsan, Saadet
- SpringerLink (Online service)
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Epidermolysis bullosa : basic and clinical aspects
STAT3 targeting in dystrophic epidermolysis bullosa
The Epidermolysis bullosa house in Salzburg
Topical ropivacaine for analgesia of aplasia cutis congenita in newborns with hereditary epidermolysis bullosa
Epidermolysis bullosa hereditaria
Epidermolysis bullosa hereditaria
Epidermolysis bullosa hereditaria
Inherited epidermolysis bullosa
Integra®-Dermal Regeneration Template and Split-Thickness Skin Grafting: A Therapy Approach to Correct Aplasia Cutis Congenita and Epidermolysis Bullosa in Carmi Syndrome
Krankheitsverarbeitung bei Epidermolysis bullosa hereditaria
Clinical aspects of epidermolysis bullosa : findings of the Freiburg epidermolysis bullosa registry 2003-2011
Aplasia Cutis Congenita: A Case Report
Epidermolysis bullosa : basic and clinical aspects
STAT3 targeting in dystrophic epidermolysis bullosa