Wikidata

(Q55670646)

English

Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia

article

In more languages

Statements

title
Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia (English)
0 references
author
Guy A. Rouleau
series ordinal
8
object named as
Guy A Rouleau
0 references
Patrick Cossette
series ordinal
10
object named as
Patrick Cossette
0 references
Anne Noreau
series ordinal
3
object named as
Anne Noreau
0 references
Micheline Gravel
series ordinal
6
object named as
Micheline Gravel
0 references
Maxime Cadieux-Dion
series ordinal
1
object named as
Maxime Cadieux-Dion
0 references
Caroline Meloche
series ordinal
5
object named as
Caroline Meloche
0 references
author name string
Maude Turcotte-Gauthier
series ordinal
2
0 references
Caroline Martin
series ordinal
4
0 references
Christian Allen Drouin
series ordinal
7
0 references
Dang Khoa Nguyen
series ordinal
9
0 references
publication date
April 2014
0 references
volume
71
0 references
issue
4
0 references
page(s)
470-5
0 references

Identifiers

PubMed ID
24566826
0 references
 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    Retrieved from "https://www.wikidata.org/w/index.php?title=Q55670646&oldid=2113355651"