TY  - GEN
AU  - Bonnin,N
AU  - Borel,A
AU  - Daniel,E
AU  - Tiple,A
AU  - Joubert,R
AU  - Heng,A-E
AU  - Chiambaretta,F
TI  - [Meretoja syndrome: Identification of a family and description of the corneal involvement by confocal microscopy]
SN  - 1773-0597
PY  - 2016///0317
KW  - Aged
KW  - Amyloidosis
KW  - diagnosis
KW  - Chromosome Aberrations
KW  - Cornea
KW  - pathology
KW  - Corneal Dystrophies, Hereditary
KW  - DNA Mutational Analysis
KW  - Diagnosis, Differential
KW  - Gelsolin
KW  - genetics
KW  - Genes, Dominant
KW  - Humans
KW  - Male
KW  - Microscopy, Confocal
KW  - Pedigree
KW  - Rare Diseases
N1  - Publication Type: Case Reports; Letter
UR  - https://doi.org/10.1016/j.jfo.2014.10.016
ER  -