Wikidata

(Q45037252)

English

A novel connexin 26 gene mutation associated with features of the keratitis-ichthyosis-deafness syndrome and the follicular occlusion triad

scientific article published in September 2004

In more languages

Statements

title
A novel connexin 26 gene mutation associated with features of the keratitis-ichthyosis-deafness syndrome and the follicular occlusion triad (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
15337980
retrieved
8 December 2017
author name string
Jay R Montgomery
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
15337980
retrieved
8 December 2017
Bryan L Martin
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
15337980
retrieved
8 December 2017
Maria L Turner
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
15337980
retrieved
8 December 2017
Steven M Holland
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
15337980
retrieved
8 December 2017
publication date
1 September 2004
1 reference
stated in
Europe PubMed Central
PubMed ID
15337980
retrieved
8 December 2017
page(s)
377-382
1 reference
stated in
Europe PubMed Central
PubMed ID
15337980
retrieved
8 December 2017

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