Wikidata

(Q43964372)

English

A newly identified chromosomal microdeletion and an N-box mutation of the AChR epsilon gene cause a congenital myasthenic syndrome

scientific article published in May 2002

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Statements

title
A newly identified chromosomal microdeletion and an N-box mutation of the AChR epsilon gene cause a congenital myasthenic syndrome (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11960891
retrieved
28 November 2017
author name string
Rolf Stucka
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
11960891
retrieved
28 November 2017
Carolin Schmidt
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
11960891
retrieved
28 November 2017
Alexandre Briguet
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
11960891
retrieved
28 November 2017
Sebastian Höpfner
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
11960891
retrieved
28 November 2017
In-Ho Song
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
11960891
retrieved
28 November 2017
Dieter Pongratz
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed ID
11960891
retrieved
28 November 2017
Wolfgang Müller-Felber
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed ID
11960891
retrieved
28 November 2017
Markus A Ruegg
series ordinal
9
1 reference
stated in
Europe PubMed Central
PubMed ID
11960891
retrieved
28 November 2017
issue
Pt 5
1 reference
stated in
Europe PubMed Central
PubMed ID
11960891
retrieved
28 November 2017
page(s)
1005-1013
1 reference
stated in
Europe PubMed Central
PubMed ID
11960891
retrieved
28 November 2017

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