Hypoparathyroidism, sensorineural deafness, and renal dysgenesis syndrome with a mutation
Hypoparathyroidism, sensorineural deafness, and renal dysgenesis syndrome is an autosomal dominant disease caused by mutations in the GATA3 gene on chromosome 10p15. We identified a patient diagnosed with hypoparathyroidism who also had a family history of hypoparathyroidism and sensorineural deafne...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Korean Society of Pediatric Endocrinology,
2015-03-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |