Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia (Orphanet Journal of Rare Diseases, (2012), 7, 1, (67), 10.1186/1750-1172-7-67);Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

Orphanet Journal of Rare Diseases

Volumn 7, Issue 1, 2012, Pages

  Huang, Lijia ^a   Chardon, Jodi Warman ^a   Carter, Melissa T ^b   Friend, Kathie L ^c   Dudding, Tracy E ^d,e   Schwartzentruber, Jeremy ^f   Zou, Ruobing ^g   Schofield, Peter W ^e   Douglas, Stuart ^a   Bulman, Dennis E ^g,h   Boycott, Kym M ^a  

^a CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c WOMEN S AND CHILDREN S HOSPITAL   (Australia)

^d Hunter Genetics   (Australia)

^e UNIVERSITY OF NEWCASTLE   (Australia)

^f MCGILL UNIVERSITY   (Canada)

^g OTTAWA HOSPITAL RESEARCH INSTITUTE   (Canada)

^h UNIVERSITY OF OTTAWA   (Canada)

Author keywords

Cerebellar atrophy; Congenital nonprogressive spinocerebellar ataxia; Gene identification; ITPR1; Spinocerebellar ataxia type 29

Indexed keywords

ARTICLE; AUSTRALIA; CANADA; CLINICAL FEATURE; CONTROLLED STUDY; GENE; GENE FUNCTION; GENE IDENTIFICATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENOTYPE; HUMAN; ITPR1 GENE; MISSENSE MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; SPINOCEREBELLAR DEGENERATION;

EID: 84866143212     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/s13023-022-02297-7     Document Type: Erratum

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