Diagnostic assay for Wiskott-Aldrich syndrome and genetically related disorders
AssigneeChildren's Hospital Medical Center
InventorsKejian Zhang, Richard J. Wenstrup, Alexandra H. Filipovich
Life of this patent
Estimating the term…
Loading patent…
AssigneeChildren's Hospital Medical Center
InventorsKejian Zhang, Richard J. Wenstrup, Alexandra H. Filipovich
Estimating the term…
The methods and compositions of the invention find use in the clinical diagnosis of primary immunodeficiencies, particularly Wiskott-Aldrich related syndromes. The compositions of the invention include isolated nucleic acid molecules and oligonucleotide pairs suitable for use in amplifying regions of the Wiskott-Aldrich syndrome protein gene and in determining the nucleotide sequence of the Wiskott-Aldrich syndrome protein gene in a patient. The invention facilitates efficient, cost-effective amplification of one or more regions of the Wiskott-Aldrich syndrome protein gene. The nucleotide sequence of amplified DNA comprising one or more regions of the Wiskott-Aldrich Syndrome Protein gene can be determined using the methods and compositions of the invention. Knowledge of the patient's nucleotide sequence in the Wiskott-Aldrich Syndrome Protein gene allows diagnosis of the patient's primary immunodeficiency.
An isolated nucleic acid molecule consisting of a nucleotide sequence selected from the group consisting of:
An oligonucleotide pair comprising a first nucleic acid molecule and a second nucleic acid molecule, wherein said first nucleic acid molecule consisting of the nucleotide sequence set forth in SEQ ID No:
A kit for performing a method of amplifying a region of the Wiskott-Aldrich syndrome protein gene comprising an oligonucleotide pair consisting of:
Dependencies are inferred from the claim text.