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List of works by Christine Zühlke

Aprataxin mutations are a rare cause of early onset ataxia in Germany

scientific article

Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations

scientific article published on 10 July 2013

Early onset and slow progression of SCA28, a rare dominant ataxia in a large four-generation family with a novel AFG3L2 mutation

scientific article

Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2.

scientific article published on 11 September 2009

Isolation and in vitro cultivation turns cells from exocrine human pancreas into multipotent stem-cells

scientific article

Missense exchanges in the TTBK2 gene mutated in SCA11.

scientific article

Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxias

scientific article

Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4

scientific article (publication date: February 2004)

Spectrin mutations cause spinocerebellar ataxia type 5.

scientific article

Spinocerebellar ataxia type 17 is caused by mutations in the TATA-box binding protein

scientific article

Spinocerebellar ataxia type 17: report of a family with reduced penetrance of an unstable Gln49 TBP allele, haplotype analysis supporting a founder effect for unstable alleles and comparative analysis of SCA17 genotypes

scientific article

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