Wikidata

(Q43984990)

English

Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family

scientific article

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Statements

title
Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
23562494
retrieved
28 November 2017
author name string
E Vaillant
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
23562494
retrieved
28 November 2017
J Philippe
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
23562494
retrieved
28 November 2017
B Skrobek
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
23562494
retrieved
28 November 2017
S Lobbens
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
23562494
retrieved
28 November 2017
M Huyvaert
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed ID
23562494
retrieved
28 November 2017
R Scharfmann
series ordinal
10
1 reference
stated in
Europe PubMed Central
PubMed ID
23562494
retrieved
28 November 2017
M Polak
series ordinal
11
1 reference
stated in
Europe PubMed Central
PubMed ID
23562494
retrieved
28 November 2017
M Abdul-Rasoul
series ordinal
12
1 reference
stated in
Europe PubMed Central
PubMed ID
23562494
retrieved
28 November 2017
M Vaxillaire
series ordinal
14
1 reference
stated in
Europe PubMed Central
PubMed ID
23562494
retrieved
28 November 2017
publication date
4 April 2013
1 reference
stated in
Europe PubMed Central
PubMed ID
23562494
retrieved
28 November 2017
page(s)
276-280
1 reference
stated in
Europe PubMed Central
PubMed ID
23562494
retrieved
28 November 2017

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