[HTML][HTML] SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

S Anwar, S Riazuddin, ZM Ahmed, S Tasneem… - Journal of human …, 2009 - nature.com
Pendred's syndrome (PDS) is an autosomal-recessive disorder characterized by
sensorineural hearing loss and goiter. PDS is caused by mutations of the SLC26A4 gene …

[PDF][PDF] SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

AJ Griffith, TB Friedman, S Riazuddin - Journal of Human Genetics, 2009 - academia.edu
To date, more than 150 SLC26A4 mutations have been identified in patients with PDS,
DFNB4 or enlarged vestibular aqueduct. 9 The most prevalent mutations tend to be specific …

[PDF][PDF] SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

AJ Griffith, TB Friedman… - Journal of Human Genetics, 2009 - researchgate.net
To date, more than 150 SLC26A4 mutations have been identified in patients with PDS,
DFNB4 or enlarged vestibular aqueduct. 9 The most prevalent mutations tend to be specific …

SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

S Anwar, S Riazuddin, ZM Ahmed… - Journal of human …, 2009 - pubmed.ncbi.nlm.nih.gov
Pendred's syndrome (PDS) is an autosomal-recessive disorder characterized by
sensorineural hearing loss and goiter. PDS is caused by mutations of the SLC26A4 gene …

[引用][C] SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

S Anwar, S Riazuddin, ZM Ahmed - … of human genetics/Japan Society of …, 2009 - cir.nii.ac.jp
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in
Pakistanis | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 …

SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

A Saima, R Saima, ZM Ahmed, T Saba… - Journal of Human …, 2009 - search.proquest.com
Pendred's syndrome (PDS) is an autosomal-recessive disorder characterized by
sensorineural hearing loss and goiter. PDS is caused by mutations of the SLC26A4 gene …

SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.

S Anwar, S Riazuddin, ZM Ahmed… - Journal of Human …, 2009 - search.ebscohost.com
Pendred's syndrome (PDS) is an autosomal-recessive disorder characterized by
sensorineural hearing loss and goiter. PDS is caused by mutations of the SLC26A4 gene …

SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.

S Anwar, S Riazuddin, ZM Ahmed… - Journal of Human …, 2009 - europepmc.org
Pendred's syndrome (PDS) is an autosomal-recessive disorder characterized by
sensorineural hearing loss and goiter. PDS is caused by mutations of the SLC26A4 gene …

SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

S Riazuddin, S Anwar, S Riazuddin… - Journal of Human …, 2009 - pure.johnshopkins.edu
Pendred's syndrome (PDS) is an autosomal-recessive disorder characterized by
sensorineural hearing loss and goiter. PDS is caused by mutations of the SLC26A4 gene …

[PDF][PDF] SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

AJ Griffith, TB Friedman, S Riazuddin - Journal of Human Genetics, 2009 - academia.edu
To date, more than 150 SLC26A4 mutations have been identified in patients with PDS,
DFNB4 or enlarged vestibular aqueduct. 9 The most prevalent mutations tend to be specific …