The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathy.
Document Type
Article
Publication Date
3-2011
Keywords
Adult, Alstrom Syndrome, Biopsy, DNA Mutational Analysis, Female, Genetic Predisposition to Disease, Haplotypes, Heredity, Humans, Male, Middle Aged, Mutation, Nephritis, Interstitial, Pedigree, Phenotype, Proteins
JAX Location
Reprint Collection
JAX Source
Kidney Int 2011 Mar; 79(6):691-2.
PMID
21358663
Volume
79
Issue
6
First Page
691
Last Page
692
ISSN
1523-1755
Recommended Citation
Izzi C,
Maffei P,
Milan G,
Tardanico R,
Foini P,
Marshall J,
Marega A,
Scolari F.
The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathy. Kidney Int 2011 Mar; 79(6):691-2.
COinS