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3FC1.5 Biotin-responsive basal ganglia disease: New features in two Spanish siblings with mutations in the second thiamine transporter gene SLC19A3

✍ Scribed by M. Serrano; V. González; M. Pineda; E. Fernandez-Alvarez; R. Artuch; L. Martorell; F. Sedel; C. Depienne; B. Perez-Dueñas


Book ID
114360336
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
38 KB
Volume
15
Category
Article
ISSN
1090-3798

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