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Volume 54, Issue 3
A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima
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Genome-wide studies
Original article
A novel
TRAPPC11
mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima
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