Full text
PDF
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Cobben J. M., van der Steege G., Grootscholten P., de Visser M., Scheffer H., Buys C. H. Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy. Am J Hum Genet. 1995 Oct;57(4):805–808. [PMC free article] [PubMed] [Google Scholar]
- Hahnen E., Forkert R., Marke C., Rudnik-Schöneborn S., Schönling J., Zerres K., Wirth B. Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals. Hum Mol Genet. 1995 Oct;4(10):1927–1933. doi: 10.1093/hmg/4.10.1927. [DOI] [PubMed] [Google Scholar]
- Kausch K., Müller C. R., Grimm T., Ricker K., Rietschel M., Rudnik-Schöneborn S., Zerres K. No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers. Hum Genet. 1991 Jan;86(3):317–318. doi: 10.1007/BF00202419. [DOI] [PubMed] [Google Scholar]
- Lefebvre S., Bürglen L., Reboullet S., Clermont O., Burlet P., Viollet L., Benichou B., Cruaud C., Millasseau P., Zeviani M. Identification and characterization of a spinal muscular atrophy-determining gene. Cell. 1995 Jan 13;80(1):155–165. doi: 10.1016/0092-8674(95)90460-3. [DOI] [PubMed] [Google Scholar]
- Rudnik-Schöneborn S., Wirth B., Zerres K. Evidence of autosomal dominant mutations in childhood-onset proximal spinal muscular atrophy. Am J Hum Genet. 1994 Jul;55(1):112–119. [PMC free article] [PubMed] [Google Scholar]