Wikidata

(Q43225506)

English

A new case of creatine transporter deficiency associated with mild clinical phenotype and a novel mutation in the SLC6A8 gene

scientific article published on 30 November 2009

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Statements

title
A new case of creatine transporter deficiency associated with mild clinical phenotype and a novel mutation in the SLC6A8 gene (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
20002129
retrieved
16 November 2017
author name string
Patricia Alcaide
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
20002129
retrieved
16 November 2017
Pilar Rodriguez-Pombo
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
20002129
retrieved
16 November 2017
Pedro Ruiz-Sala
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
20002129
retrieved
16 November 2017
Isaac Ferrer
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
20002129
retrieved
16 November 2017
Pedro Castro
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
20002129
retrieved
16 November 2017
Yolanda Ruiz Martin
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
20002129
retrieved
16 November 2017
Begoña Merinero
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed ID
20002129
retrieved
16 November 2017
Magdalena Ugarte
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed ID
20002129
retrieved
16 November 2017
publication date
30 November 2009
1 reference
stated in
Europe PubMed Central
PubMed ID
20002129
retrieved
16 November 2017
page(s)
215-217
1 reference
stated in
Europe PubMed Central
PubMed ID
20002129
retrieved
16 November 2017

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