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Nephrology Dialysis Transplantation

Volumn 23, Issue 3, 2008, Pages 1071-1072

  Ardalan, Mohammad R ^a   Shoja, Mohammadali M ^b  

^a TABRIZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b TABRIZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

GELSOLIN;

AMYLOIDOSIS; AUTOSOMAL DOMINANT INHERITANCE; BLINDNESS; CHROMOSOME 9Q; DEVELOPING COUNTRY; FAMILY STUDY; GENE LOCUS; GENE MUTATION; HUMAN; IRAN; IRELAND; LETTER; MENTAL STRESS; PERCEPTION DEAFNESS; PRIORITY JOURNAL; RARE DISEASE; RETINITIS PIGMENTOSA;

EID: 44449176583     PISSN: 09310509     EISSN: 14602385     Source Type: Journal    
DOI: 10.1093/ndt/gfm586     Document Type: Letter

References (3)

1. Ardalan MR, Shoja MM, Kiuru-Enari S. Amyloidosis-related nephrotic syndrome due to a G654A gelsolin mutation: the first report from the Middle East. Nephrol Dial Transplant 2007; 22: 272-275
2. Ardalan MR, Shoja MM, Paunio T et al. Hereditary gelsolin amyloidosis in Iran. In: Skinner M, et al. eds. XIth International Symposium on Amyloidosis. CRC Press, USA: 2007
3. Kenna P, Mansergh F, Millington-Ward S et al. Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness. Br J Ophthalmol 1997; 81: 207-213