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SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6 (disorder)
Known as:
CEREBELLAR ATAXIA, INFANTILE NONPROGRESSIVE, AUTOSOMAL RECESSIVE
, SCAR6
, Spinocerebellar ataxia, autosomal recessive 6
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National Institutes of Health
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Related topics
Related topics
9 relations
Action Tremor
Autosomal recessive inheritance
CLA3 gene
Clumsiness
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Broader (1)
Spinocerebellar Degeneration
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Erratum: A Novel Missense Mutation in ADAMTS10 in Norwegian Elkhound Primary Glaucoma (PLoS ONE (2014) 9:11 (e111941) DOI: 10.1371/journal.pone.0111941)
S. Ahonen
,
Maria Kaukonen
,
F. Nussdorfer
,
Christine D Harman
,
A. Komáromy
,
H. Lohi
2015
Corpus ID: 196452127
2015
2015
Rochelle salt – a structural reinvestigation with improved tools. I. The high-temperature paraelectric phase at 308 K
F. Mo
,
R. Mathiesen
,
J. A. Beukes
,
K. M. Vu
IUCrJ
2015
Corpus ID: 18041212
A novel sample cell with control of temperature and relative humidity permitted collection of data of excellent quality, enabling…
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2015
2015
Nanoencapsulação de compostos de rutênio, análise de sua atividade anti - Mycobacterium tuberculosis e biodisponibilidade oral
Eduardo Sinesio de Freitas
2015
Corpus ID: 78012218
Tuberculosis (TB) is an infectious airborne disease, curable and mainly affects the lungs. In recent years, the death rate has…
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2010
2010
Dynamic bilateral arytenoid and vocal fold collapse associated with head flexion in 5 Norwegian Coldblooded Trotter racehorses
E. Strand
,
S. Hanche‐olsen
,
A. Grønvold
,
C. N. Mellum
2010
Corpus ID: 72822864
Dynamic obstruction of the upper airway is a common cause of poor performance in racehorses, often associated with abnormal…
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2010
2010
Deletion of the Chd6 exon 12 affects motor coordination
M. J. Lathrop
,
L. Chakrabarti
,
+8 authors
S. Fiering
Mammalian Genome
2010
Corpus ID: 6137237
Members of the CHD protein family play key roles in gene regulation through ATP-dependent chromatin remodeling. This is…
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2007
2007
The coding region of TP53INP2, a gene expressed in the developing nervous system, is not altered in a family with autosomal recessive non‐progressive infantile ataxia on chromosome 20q11‐q13
Jennifer S. Bennetts
,
N. D. Rendtorff
,
Fiona Simpson
,
L. Tranebjaerg
,
C. Wicking
Developmental Dynamics
2007
Corpus ID: 45461409
The locus for autosomal recessive infantile cerebellar ataxia (CLA3 or SCAR6) has been mapped to chromosome 20q11‐q13 in a single…
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2005
2005
Evaluation of canine COL4A3 and COL4A4 as candidates for familial renal disease in the Norwegian elkhound.
A. C. Wiersma
,
L. Millon
,
A. M. V. Dongen
,
B. A. V. Oost
,
D. Bannasch
Journal of Heredity
2005
Corpus ID: 25171251
The collagen type IV alpha3 and alpha4 chains (COL4A3 and COL4A4) are part of the specialized glomerular basement membrane in the…
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Highly Cited
1987
Highly Cited
1987
Retinal degenerations in the dog: IV. Early retinal degeneration (erd) in Norwegian elkhounds.
G. Acland
,
G. D. Aguirre
,
G. D. Aguirre
Experimental Eye Research
1987
Corpus ID: 23081282
1982
1982
Chondrodysplasia in the Norwegian Elkhound.
S. Bingel
,
R. Sande
American Journal of Pathology
1982
Corpus ID: 25144408
Dwarfism in the Norwegian Elkhound occurred as a result of a generalized disturbance in endochondral ossification. Radiographic…
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1977
1977
Intracutaneous cornifying epithelioma ("keratoacanthoma") of dogs and keratoacanthoma of man.
R. Rudolph
,
A. P. Gray
,
H. Leipold
The Cornell veterinarian
1977
Corpus ID: 40435844
The intracutaneous cornifying epithelioma ("keratoacanthoma") of dogs was compared with keratoacanthoma of man based on findings…
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