Clinical utility gene card for: Alström syndrome.

Document Type

Article

Publication Date

10-2011

Keywords

Alstrom Syndrome, Cardiomyopathies, Child, Child, Preschool, Diagnosis, Differential, Female, Genetic Testing, Genotype, Humans, Infant, Male, Mutation, Phenotype, Proteins, Retinal Degeneration, Sensitivity and Specificity

JAX Source

Eur J Hum Genet 2011 Oct; 19(10).

PMID

21522186

Volume

19

Issue

10

ISSN

1476-5438

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