Published in
BioMed Central, Orphanet Journal of Rare Diseases, 1(12), 2017
DOI: 10.1186/s13023-017-0672-7
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Spinocerebellar ataxia type 29 due to mutations in ITPR1: A case series and review of this emerging congenital ataxia
Journal article published in 2017 by
Jessica L. Zambonin,
Allison Bellomo,
Hilla Ben-Pazi,
David B. Everman,
Lee M. Frazer,
Michael T. Geraghty,
Amy D. Harper,
Julie R. Jones,
Benjamin Kamien,
Kristin Kernohan,
Mary Kay Koenig,
Matthew Lines,
Elizabeth Emma Palmer 
,
Randal Richardson,
Reeval Segel
and other authors.
,
Randal Richardson,
Reeval Segel
and other authors.
This paper is made freely available by the publisher.
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