Phenotypic variability of TTR Val122Ile mutation: a Caucasian patient with axonal neuropathy and normal heart
Neurol Sci
.
2017 Mar;38(3):525-526.
doi: 10.1007/s10072-016-2767-7.
Epub 2016 Nov 12.
Authors
Claudia Stancanelli
1
2
3
,
Luca Gentile
4
,
Gianluca Di Bella
4
,
Fabio Minutoli
5
,
Massimo Russo
6
,
Giuseppe Vita
4
,
Anna Mazzeo
4
Affiliations
1
Biomedical Department of Internal Medicine and Specialistic, University of Palermo, Palermo, Italy. claudia.stancanelli@yahoo.it.
2
Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy. claudia.stancanelli@yahoo.it.
3
UOC Neurologia e Malattie Neuromuscolari, AOU Policlinico Gaetano Martino, Via consolare valeria 1, 98127, Messina, Italy. claudia.stancanelli@yahoo.it.
4
Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
5
Department of Biomedical and Dental Sciences and of Morphological and Functional Images, University of Messina, Messina, Italy.
6
Nemo Sud Clinical Centre, AOU Policlinico, Messina, Italy.
PMID:
27838833
DOI:
10.1007/s10072-016-2767-7
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Aged
Humans
Male
Mutation
Peripheral Nervous System Diseases / genetics*
Peripheral Nervous System Diseases / physiopathology
Phenotype
Prealbumin / genetics*
White People / genetics
Substances
Prealbumin