Title

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

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