Publication | Closed Access
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene
382
Citations
20
References
2001
Year
New HitMendelian DisorderOphthalmologyGenetic DisorderGeneticsOcular Motor ApraxiaDegenerative DiseaseMotor DisorderEarly-onset AtaxiaNeurologyDisease Gene IdentificationNeuropathologyMedicine
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