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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.
Highly Cited
2015
Highly Cited
2015
Phytoplankton dynamics in contrasting early stage North Atlantic spring blooms: composition, succession, and potential drivers
C. Daniels
,
A. Poulton
,
+4 authors
Adrian P. Martin
2015
Corpus ID: 17807235
Abstract. The spring bloom is a key annual event in the phenology of pelagic ecosystems, making a major contribution to the…
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2014
2014
A Novel Missense Mutation in ADAMTS10 in Norwegian Elkhound Primary Glaucoma
S. Ahonen
,
Maria Kaukonen
,
F. Nussdorfer
,
Christine D Harman
,
A. Komáromy
,
H. Lohi
PLoS ONE
2014
Corpus ID: 8567516
Primary glaucoma is one of the most common causes of irreversible blindness both in humans and in dogs. Glaucoma is an optic…
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Highly Cited
2013
Highly Cited
2013
Start codon targeted (SCoT) polymorphism in toxic and non-toxic accessions of Jatropha curcas L. and development of a codominant SCAR marker.
Sujatha Mulpuri
,
Tarakeswari Muddanuru
,
G. Francis
Plant Science
2013
Corpus ID: 1676706
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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2004
2004
Ocular histopathologic observations in Norwegian Elkhounds with primary open-angle, closed-cleft glaucoma.
Y. Oshima
,
E. Bjerkås
,
R. Peiffer
Veterinary Ophthalmology
2004
Corpus ID: 45445979
A retrospective histopathologic study of primary glaucoma in the Norwegian Elkhound was undertaken with the study of 9 clinically…
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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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