MOLECULAR GENETIC ANALYSIS OF HEREDITARY MOTOR AND SENSORY NEUROPATHIES
- 2 Anni 1995/1997
- 36.152€ Totale Fondi
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Pubblicazioni Scientifiche
- 1996 HUMAN MUTATION
Identification of a 4 bp deletion (1560del4) in Po gene in a family with severe Charcot-Marie-Tooth disease
- 1997 NEUROLOGY
Underexpression of messenger RNA for peripheral myelin protein 22 in hereditary neuropathy with liability to pressure palsies
- 1996 NEUROSCIENCE LETTERS
Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: A reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patients
- 1996 AMERICAN JOURNAL OF HUMAN GENETICS
De novo duplication in Charcot-Marie-Tooth type 1A
