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The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

Author
JAY, P1 ; ROUGEULLE, C2 ; BERTA, P1 ; LALANDE, M2 ; MUSCATELLI, F4 ; MASSACRIER, A3 ; MONCLA, A4 ; MATTEI, M.-G4 ; MALZAC, P4 ; ROËCKEL, N4 ; TAVIAUX, S1 ; LEFRANC, J.-L. B4 ; CAU, P3
[1] Centre de Recherches de Biochimie Macromoléculaire, CNRS ERS 115, INSERM U 249, route de Mende, BP 5051, 34033 Montpellier, France
[2] Genetics Division, Children's Hospital, Harvard Medical School and Howard Hughes Medical Institute, 300 Longwood Avenue, Boston, Massachusetts 02115, United States
[3] Laboratoire de Biologie cellulaire, 27 Bvd. Jean Moulin, 13385 Marseille, France
[4] Unité INSERM 406, 27 Bvd. Jean Moulin, 13385 Marseille, France
Source

Nature genetics. 1997, Vol 17, Num 3, pp 357-361 ; ref : 31 ref

CODEN
NGENEC
ISSN
1061-4036
Scientific domain
Genetics
Publisher
Nature Publishing Group, London
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Chromosome D15 Empreinte génomique Expression génique Gène Génétique Homme Homologie Origine paternelle Prader Labhart Willi syndrome Région critique Système nerveux central Séquence nucléotide Necdine Appareil génital pathologie Arriération mentale Maladie héréditaire Syndrome complexe Système nerveux pathologie
Keyword (en)
Chromosome D15 Genomic imprinting Gene expression Gene Genetics Human Homology Paternal origin Prader Labhart Willi syndrome Critical region Central nervous system Nucleotide sequence Genital diseases Mental retardation Genetic disease Complex syndrome Nervous system diseases
Keyword (es)
Cromosoma D15 Huella genómica Expresión genética Gen Genética Hombre Homología Origen paterno Prader Labhart Willi síndrome Región crítica Sistema nervioso central Secuencia nucleótido Aparato genital patología Retraso mental Enfermedad hereditaria Síndrome complejo Sistema nervioso patología
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23E Complex syndromes

Discipline
Medical genetics
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
2055525

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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