Infantile presentation of the mitochondrial A8344G mutation.

Scalais, E; Nuttin, C.; Seneca, S.; Smet, J.; De Paepe, B.; Martin, J. J.; Stevens, R.; Pierart, F.; Battisti, Oreste; Lissens, W; De Merleir, L; Van Coster, R

doi:10.1111/j.1468-1331.2007.01926.x

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Article (Scientific journals)

Infantile presentation of the mitochondrial A8344G mutation.

Scalais, E; Nuttin, C.; Seneca, S. et al.

2007 • In European Journal of Neurology, 14, p. 3-5

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https://hdl.handle.net/2268/18930

DOI
10.1111/j.1468-1331.2007.01926.x

PubMed
17956438

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Disciplines :

Neurology

Author, co-author :

Scalais, E

Nuttin, C.

Seneca, S.

Smet, J.

De Paepe, B.

Martin, J. J.

Stevens, R.

Pierart, F.

Battisti, Oreste ; Université de Liège > Département des sciences cliniques > Pédiatrie

Lissens, W

De Merleir, L

Van Coster, R

Language :

English

Title :

Infantile presentation of the mitochondrial A8344G mutation.

Publication date :

2007

Journal title :

European Journal of Neurology

ISSN :

1351-5101

eISSN :

1468-1331

Publisher :

Blackwell Science, Oxford, United Kingdom

Volume :

Pages :

3-5

Peer reviewed :

Peer Reviewed verified by ORBi

Available on ORBi :

since 17 August 2009

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Bibliography

De Paepe B, Smet J, Leroy JG, et al. Diagnostic value of immunostaining in cultured skin fibroblasts from patients with oxidative phosphorylation defects. Pediatric Research 2006 59:1 5.