A family with hypoparathyroidism, sensorineural deafness and renal disease (Barakat syndrome) caused by a reduced gene dosage in GATA3

Please use this identifier to cite or link to this item: http://repo.jfn.ac.lk/med/handle/701/1846

Full metadata record

DC Field	Value	Language
dc.contributor.author	Joseph, Anne D. D.	-
dc.contributor.author	Sirisena, Nirmala D.	-
dc.contributor.author	Kumanan, T.	-
dc.contributor.author	Sujanitha, Vathulan	-
dc.date.accessioned	2019-03-07T05:28:41Z	-
dc.date.accessioned	2022-09-16T10:26:42Z	-
dc.date.available	2019-03-07T05:28:41Z	-
dc.date.available	2022-09-16T10:26:42Z	-
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.jfn.ac.lk/med/handle/701/1846	-
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
Appears in Collections:	Medicine

Files in This Item:

File	Description	Size	Format
Abstract application form_BS abstract-1 (1).pdf		336.99 kB	Adobe PDF	View/Open