Modification of CMT1 Phenotypes by the Independent Coexisting Neurogenetic Disorders, McArdle Disease and Chromosome 5p Trisomy

Journal article

Peer reviewed

FLORIAN P. Thomas, THOMAS J. Geller, ANGELIKA F. Hahn, LUDWIG Gutmann, XIN-LI Huang, HUI WU, HERMAN E. Wyandt and ROGER V. Lebo

Annals of the New York Academy of Sciences, Vol.883(1), pp.472-476

10/1999

DOI: 10.1111/j.1749-6632.1999.tb08614.x

PMID: 10586277

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Title: Subtitle: Modification of CMT1 Phenotypes by the Independent Coexisting Neurogenetic Disorders, McArdle Disease and Chromosome 5p Trisomy
Creators: FLORIAN P. Thomas - Department of Neurology, Saint Louis University School of Medicine, St. Louis, Missouri 63110-0250, USA
THOMAS J. Geller - Department of Neurology, Saint Louis University School of Medicine, St. Louis, Missouri 63110-0250, USA
ANGELIKA F. Hahn - Department of Neurology, University of Western Ontario, London, Ontario N6A 5A5, Canada
LUDWIG Gutmann - West Virginia University
XIN-LI Huang - Center for Human Genetics, Boston University, Boston, Massachusetts 02118-2394, USA
HUI WU - Department of Neurology, Saint Louis University School of Medicine, St. Louis, Missouri 63110-0250, USA
HERMAN E. Wyandt - Center for Human Genetics, Boston University, Boston, Massachusetts 02118-2394, USA
ROGER V. Lebo - Center for Human Genetics, Boston University, Boston, Massachusetts 02118-2394, USA
Resource Type: Journal article
Publication Details: Annals of the New York Academy of Sciences, Vol.883(1), pp.472-476
DOI: 10.1111/j.1749-6632.1999.tb08614.x
PMID: 10586277
NLM abbreviation: Ann N Y Acad Sci
ISSN: 0077-8923
eISSN: 1749-6632
Publisher: Blackwell Publishing Ltd
Number of pages: 5
Language: English
Date published: 10/1999
Academic Unit: Neurology
Record Identifier: 9984303447102771

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