Hypoparathyroidism, sensorineural deafness and renal dysplasia

GATA3 - hypoparathyroidism, sensorineural deafness, and renal dysplasia

This test is available for the following conditions:

• Conditions > Hearing impairment > Hypoparathyroidism, sensorineural deafness and renal dysplasia
• Conditions > Endocrine > Hypoparathyroidism, sensorineural deafness and renal dysplasia
• Conditions > Renal / Nephrological > Hypoparathyroidism, sensorineural deafness and renal dysplasia

This product is also part of the following panels:

• WES hearing impairment (including GJB2) (100.0% *)
• WES Mendelian inherited disorders (100.0% *)
• WES Mendelian inherited disorders (100.0% *)
• WES renal disorders (100.0% *)
• WES renal disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

• Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 131320
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

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