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Modification of CMT1 Phenotypes by the Independent Coexisting Neurogenetic Disorders, McArdle Disease and Chromosome 5p Trisomy
FLORIAN P. THOMAS, THOMAS J. GELLER, ANGELIKA F. HAHN, LUDWIG GUTMANN, XIN-LI HUANG, HUI WU, HERMAN E. WYANDT, ROGER V. LEBOVolume:
883
Year:
1999
Pages:
5
DOI:
10.1111/j.1749-6632.1999.tb08614.x
File:
PDF, 1.50 MB
1999