Wikidata

(Q42435194)

English

A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination

scientific article published on 22 April 2008

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Statements

title
A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
18430779
retrieved
31 October 2017
author name string
Bruce L Patton
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
18430779
retrieved
31 October 2017
Bing Wang
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
18430779
retrieved
31 October 2017
Yukie S Tarumi
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
18430779
retrieved
31 October 2017
Kevin L Seburn
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
18430779
retrieved
31 October 2017
publication date
22 April 2008
1 reference
stated in
Europe PubMed Central
PubMed ID
18430779
retrieved
31 October 2017
issue
Pt 10
1 reference
stated in
Europe PubMed Central
PubMed ID
18430779
retrieved
31 October 2017
page(s)
1593-1604
1 reference
stated in
Europe PubMed Central
PubMed ID
18430779
retrieved
31 October 2017

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