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

Overview of attention for article published in Orphanet Journal of Rare Diseases, April 2015

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PubMed: Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype. http://t.co/C3vPKMlEw8

New OJRD article expands phenotype of TTC19 deficiency - a progressive neurodegenerative disease http://t.co/6xf25vzmYM #RareDisease

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