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Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathies. Commentary

Author
DEBIEC, Hanna1 ; NAUTA, Jeroen2 ; KERJASCHKI, Dontscho (Commentator) 8 ; COULET, Florence3 ; VAN DER BURG, Mirjam4 ; GUIGONIS, Vincent5 ; SCHURMANS, Thierry6 ; DE HEER, Emile7 ; SOUBRIER, Florent3 ; JANSSEN, Francoise6 ; RONCO, Pierre1
[1] INSERM Unit 489, Tenon Hospital (AP-HP) and University of Paris 6, Paris, France
[2] Sophia Children's Hospital, Erasmus MC, Rotterdam, Netherlands
[3] Department of Human Genetics, Tenon Hospital (AP-HP) and University of Paris 6, Paris, France
[4] Department of Immunology, Erasmus MC, Rotterdam, Netherlands
[5] Department of Pediatric Nephrology, ArmandTrousseau Hospital (AP-HP), Paris, France
[6] Department of Pediatric Nephrology, Brussels Free University, Brussels, Belgium
[7] Department of Pathology, Leiden University Medical Centre, Leiden, Netherlands
[8] Department of Pathology, Medical University of Vienna, Allgemeines Krankenhaus, 1090 Wien, Austria
Source

Lancet (British edition). 2004, Vol 364, Num 9441, pp 1194-1196, 11 p ; ref : 50 ref

CODEN
LANCAO
ISSN
0140-6736
Scientific domain
General medicine general surgery
Publisher
Lancet, London
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Etude critique Foetomaternel Gène Génétique Mutation Médecine Prénatal
Keyword (en)
Critical study Fetomaternal Gene Genetics Mutation Medicine Prenatal
Keyword (es)
Estudio crítico Fetomaternal Gen Genética Mutación Medicina Prenatal
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B01 General aspects

Discipline
Generalities in medical sciences
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
16157047

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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