A family with hypoparathyroidism, sensorineural deafness and renal disease (Barakat syndrome) caused by a reduced gene dosage in GATA3
| dc.contributor.author | Joseph Anne, D.D. | |
| dc.contributor.author | Sirisena Nirmala, D. | |
| dc.contributor.author | Kumanan, T. | |
| dc.contributor.author | Sujanitha, V. | |
| dc.date.accessioned | 2022-09-26T05:40:47Z | |
| dc.date.available | 2022-09-26T05:40:47Z | |
| dc.date.issued | 2019 | |
| dc.identifier.citation | 3rd Annual Rare Disease Day Symposium 2019, 28th February 2019 at New Auditorium of Lady Ridgeway Children’s Hospital, Colombo, Sri Lanka. | en_US |
| dc.identifier.uri | http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/7514 | |
| dc.language.iso | en | en_US |
| dc.publisher | Rare Disease Forum of the Sri Lanka College of Paediatricians | en_US |
| dc.subject | Hypoparathyroidism | en_US |
| dc.subject | Renal disease | en_US |
| dc.subject | Barakat syndrome | en_US |
| dc.subject | Sensorineural deafness | en_US |
| dc.title | A family with hypoparathyroidism, sensorineural deafness and renal disease (Barakat syndrome) caused by a reduced gene dosage in GATA3 | en_US |
| dc.type | Research abstract | en_US |