Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)-Reference-Cited by-同舟云学术

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

Published:1997-12 Issue:4 Volume:17 Page:411-422
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Everett Lorraine A.,Glaser Benjamin,Beck John C.,Idol Jacquelyn R.,Buchs Andreas,Heyman Ma'ayan,Adawi Faiad,Hazani Elizur,Nassir Elias,Baxevanis Andreas D.,Sheffield Val C.,Green Eric D.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1297-411.pdf

Reference74 articles.

1. Pendred, V. Deaf-mutism and goitre. Lancet ii, 532 (1896).

2. Reardon, W. & Trembath, R.C. Pendred syndrome. J. Med. Genet. 33, 1037–1040 (1996).

3. Reardon, W. et al. Pendred syndrome: 100 years of underascertainment. Q. J. Med. 90, 443–447 (1997).

4. Fraser, G.R. Association of congenital deafness with goitre (Pendred's syndrome): a study of 207 families. Ann. Hum. Genet. 28, 201–249 (1965).

5. Batsakis, J.G. & Nishiyama, R.H. Deafness with sporadic goiter. Arch. Otolaryngol. 76, 401–406 (1962).

Cited by 1015 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Risks of Iodine Excess;Endocrine Reviews;2024-06-13

2. Oligomerization and cellular localization of SLC26A11;2024-05-01

3. The molecular principles underlying diverse functions of the SLC26 family of proteins;Journal of Biological Chemistry;2024-05

4. The role of SLC26A4 in bony labyrinth development and otoconial mineralization in mouse models;Frontiers in Molecular Neuroscience;2024-04-29

5. Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia;Annals of Human Genetics;2024-03-22