A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome

Journal article

Peer reviewed

K Steindl, A. M Alazami, S. A Schneider, K. P Bhatia, J. T Wuerfel, D Petersen, R Cartolari, G Neri, C Klein, B Mongiardo, …

Clinical genetics, Vol.78(6), pp.594-597

12/2010

PMID: 21044051

Abstract

Biological and medical sciences

Fundamental and applied biological sciences. Psychology

General aspects. Genetic counseling

Genetics of eukaryotes. Biological and molecular evolution

Medical genetics

Medical sciences

Molecular and cellular biology

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Title: A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome
Creators - without role: K Steindl - Università Cattolica del Sacro Cuore
A. M Alazami - King Faisal Specialist Hospital & Research Centre
S. A Schneider - National Hospital for Neurology and Neurosurgery
K. P Bhatia - National Hospital for Neurology and Neurosurgery
J. T Wuerfel - Institute of Neurobiology
D Petersen - Institute of Neurobiology
R Cartolari - Ospedale di Belcolle
G Neri - Università Cattolica del Sacro Cuore
C Klein - University of Lübeck
B Mongiardo - Ospedale di Belcolle
F. S Alkuraya - King Faisal Specialist Hospital & Research Centre
Publication Details: Clinical genetics, Vol.78(6), pp.594-597
Publisher: Wiley-Blackwell
Identifiers: 9913541908331
Academic Unit: King Khalid University; King Faisal University; King Saud University; Alfaisal University
Language: English
Resource Type: Journal article