Wikidata

(Q34586332)

English

Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13.

scientific article

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title
Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13. (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
17139268
retrieved
3 August 2017
author name string
Caroline Lefèvre
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
17139268
retrieved
3 August 2017
Ludovic Martin
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed ID
17139268
retrieved
3 August 2017
Gianluca Tadini
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed ID
17139268
retrieved
3 August 2017
Aysen Karaduman
series ordinal
9
1 reference
stated in
Europe PubMed Central
PubMed ID
17139268
retrieved
3 August 2017
Serap Emre
series ordinal
10
1 reference
stated in
Europe PubMed Central
PubMed ID
17139268
retrieved
3 August 2017
Safa Saker
series ordinal
11
1 reference
stated in
Europe PubMed Central
PubMed ID
17139268
retrieved
3 August 2017
Judith Fischer
series ordinal
13
1 reference
stated in
Europe PubMed Central
PubMed ID
17139268
retrieved
3 August 2017
publication date
30 November 2006
1 reference
stated in
Europe PubMed Central
PubMed ID
17139268
retrieved
3 August 2017

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