(Q28140272)

4

0 references

Collette Hand

object named as

C Hand

8

0 references

0 references

19

G A Rouleau

0 references

D Laoudj

6

object named as

D Laoudj

0 references

author name string

G Munhoz Essenfelder

2

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Z Kibar

3

0 references

E Callouet

5

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G Lemaître

7

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S J Hayflick

9

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J Zonana

10

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S Antonarakis

11

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U Radhakrishna

12

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D P Kelsell

13

0 references

A L Christianson

14

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A Pitaval

15

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V Der Kaloustian

16

0 references

C Fraser

17

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C Blanchet-Bardon

18

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G Waksman

The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q

20

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language of work or name

English

0 references

publication date

October 2000

0 references

published in

Nature Genetics

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volume

26

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issue

2

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page(s)

142-4

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cites work

1 reference

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

21 April 2017

1 reference

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

21 April 2017

1 reference

Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

21 April 2017

1 reference

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment

21 April 2017

1 reference

Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping

21 April 2017

1 reference

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

21 January 2018

1 reference

Connexin 26 gene linked to a dominant deafness

21 January 2018

1 reference

Molecular cloning and functional expression of mouse connexin-30,a gap junction gene highly expressed in adult brain and skin

21 January 2018

1 reference

A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families

21 January 2018

1 reference

Hidrotic ectodermal dysplasia: a clinical and ultrastructural observation

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

A 1.5-Mb Physical Map of the Hidrotic Ectodermal Dysplasia (Clouston Syndrome) Gene Region on Human Chromosome 13q11

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Refined localization of the gene for Clouston syndrome (hidrotic ectodermal dysplasia) in a large French family

1 reference