Spinocerebellar tract Spinocerebellar ataxia Spinocerebellar ataxia type 6 X-linked sideroblastic anemia and spinocerebellar ataxia Spinocerebellar ataxia type-13 Spinocerebellar ataxia type 1 Corneal-cerebellar syndrome Machado–Joseph disease Autosomal recessive cerebellar ataxia TTBK2 ATXN8OS Aya Kitō Ataxin 10 KCNC3 Ataxin 7 Autosomal dominant cerebellar ataxia Ataxin-2 Cerebellar peduncle Posterior thoracic nucleus Ataxin 1 Troriluzole Inferior cerebellar peduncle Huntington's disease-like syndrome Interposed nucleus TDP1 Accessory cuneate nucleus Synaptotagmin-14 International Cooperative Ataxia Rating Scale SPTBN2 Paul Robert Bing PLEKHG4 …
ATXN2L Oculomotor apraxia Type 6 Truncal ataxia Polyglutamine tract TGM6 Type 13 CCDC88C (gene) Cav2.1 Lateral corticospinal tract List of diseases (S) ELOVL4 PRKCG FGF14 COA7 N. H. Wadia Boucher-Neuhäuser syndrome Twinkle (protein) Octave Crouzon A Litre of Tears (film) Zinc finger protein 592 Huda Zoghbi SCYL1 Ataxin Olivopontocerebellar atrophy Spastic ataxia-corneal dystrophy syndrome Achal Kumar Srivastava Tom Otis Kara Kennedy (canoeist) Globose nucl
eus RBFOX1 Ataxin 3 Olivary body QRICH1 Dynamic mutation Russell Terrier Sherman paradox Familial isolated vitamin E deficiency Alpha-tocopherol transfer protein Cerebellar degeneration Cerebellar ataxia Chromosome instability syndrome Scratch reflex PPP2R2B ITPR1 Somatotopic arrangement Thyrotropin-releasing hormone Gerry Neugebauer Rubicon (protein) Christianson syndrome Superior cerebellar peduncle Slipped strand mispairing Taltirelin Trinucleotide repeat disorder Dentatorubral–pallidoluysian atrophy Episodic ataxia 1 Litre no Namida (TV series) Enaptin Ludwig Edinger SCA Gustave Roussy Dissociated sensory loss Vitamin
Spinocerebellar ataxia
Spinocerebellar ataxia type 6
X-linked sideroblastic anemia and spinocerebellar ataxia
Spinocerebellar ataxia type-13
Spinocerebellar ataxia type 1
Corneal-cerebellar syndrome
Machado–Joseph disease
Autosomal recessive cerebellar ataxia
TTBK2
ATXN8OS
Aya Kitō
Ataxin 10
KCNC3
Ataxin 7
Autosomal dominant cerebellar ataxia
Ataxin-2
Cerebellar peduncle
Posterior thoracic nucleus
Ataxin 1
Troriluzole
Inferior cerebellar peduncle
Huntington's disease-like syndrome
Interposed nucleus
TDP1
Accessory cuneate nucleus
Synaptotagmin-14
International Cooperative Ataxia Rating Scale
SPTBN2
Paul Robert Bing
PLEKHG4
ATXN2L
Oculomotor apraxia
Type 6
Truncal ataxia
Polyglutamine tract
TGM6
Type 13
CCDC88C (gene)
Cav2.1