دورية أكاديمية

Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice.

التفاصيل البيبلوغرافية
العنوان: Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice.
المؤلفون: Beck TF; Department of Molecular and Human Genetics., Veenma D; Department of Pediatric Surgery.; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam 3015 GJ, The Netherlands., Shchelochkov OA; Department of Pediatrics, The University of Iowa, Iowa City, IA 52242, USA., Yu Z; Department of Molecular and Human Genetics., Kim BJ; Department of Molecular and Human Genetics., Zaveri HP; Department of Molecular and Human Genetics., van Bever Y; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam 3015 GJ, The Netherlands., Choi S; Institute for Genetic Medicine and Center for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA., Douben H; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam 3015 GJ, The Netherlands., Bertin TK; Department of Molecular and Human Genetics., Patel PI; Institute for Genetic Medicine and Center for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA., Lee B; Department of Molecular and Human Genetics.; Howard Hughes Medical Institute, Houston, TX 77030, USA., Tibboel D; Department of Pediatric Surgery., de Klein A; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam 3015 GJ, The Netherlands., Stockton DW; Department of Pediatrics.; Department of Internal Medicine, Wayne State University, Detroit, MI 48201, USA., Justice MJ; Department of Molecular and Human Genetics., Scott DA; Department of Molecular and Human Genetics.; Department of Molecular Physiology and Biophysics Baylor College of Medicine, Houston, TX 77030, USA.
المصدر: Human molecular genetics [Hum Mol Genet] 2020 Apr 15; Vol. 29 (6), pp. 1054.
نوع المنشور: Journal Article; Published Erratum
اللغة: English
بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: PubMed not MEDLINE; MEDLINE
أسماء مطبوعة: Original Publication: Oxford, England ; New York : IRL Press at Oxford University Press, c1992-
التعليقات: Erratum for: Hum Mol Genet. 2013 Mar 1;22(5):1026-38. (PMID: 23221805)
معلومات مُعتمدة: P30 HD024064 United States HD NICHD NIH HHS; R03 EY014854 United States EY NEI NIH HHS
تواريخ الأحداث: Date Created: 20200205 Latest Revision: 20210804
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC8325106
DOI: 10.1093/hmg/ddz307
PMID: 32016392
قاعدة البيانات: MEDLINE
الوصف
تدمد:1460-2083
DOI:10.1093/hmg/ddz307