Mutations in TTC19: expanding the molecular, clinical and...

Orphanet Journal of Rare Diseases 2015 / 12 Vol. 10; Iss. 1

Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype

Koch, Johannes, Freisinger, Peter, Feichtinger, René G, Zimmermann, Franz A, Rauscher, Christian, Wagentristl, Hans P, Konstantopoulou, Vassiliki, Seidl, Rainer, Haack, Tobias B, Prokisch, Holger, Aht
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Volume:
10
Language:
english
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/s13023-015-0254-5
Date:
December, 2015
File:
PDF, 2.35 MB
english, 2015
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