Surfactant Protein B Deficiency Caused by Homozygous C248X Mutation—A Case Report and Review of the Literature-Reference-Cited by-同舟云学术

Surfactant Protein B Deficiency Caused by Homozygous C248X Mutation—A Case Report and Review of the Literature

Published:2015-03-02 Issue:01 Volume:05 Page:e053-e059
ISSN:2157-6998
Container-title:American Journal of Perinatology Reports
language:en
Short-container-title:AJP Rep

Author:

Resch Bernhard¹,Kraschl Raimund²,Windpassinger Christian³,Eber Ernst⁴,Kurath-Koller Stefan⁵

Affiliation:

1. Division of Neonatology, Paediatric Department, Research Unit for Neonatal Infectious Diseases and Epidemiology, Medical University of Graz, Graz, Austria

2. Division of Neonatology, Pediatric Department, General Hospital of Klagenfurt, Klagenfurt, Austria

3. Department for human Genetics, Medical University of Graz, Graz, Austria

4. Division of Pulmonology, Paediatric Department, Medical University of Graz, Graz, Austria

5. Division of General Pediatrics, Paediatric Department, Medical University of Graz, Graz, Austria

Publisher

Georg Thieme Verlag KG

Subject

Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0035-1545668.pdf

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