Modification of CMT1 Phenotypes by the Independent...

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. LEBO
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Volume:
883
Year:
1999
Pages:
5
DOI:
10.1111/j.1749-6632.1999.tb08614.x
File:
PDF, 1.50 MB
1999
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