First case of compound heterozygosity in ALS2 gene in infantile-onset ascending spastic paralysis with bulbar involvement

L. Sztriha, C. Panzeri, R. Kálmánchey, R. Szabó, E. Endreffy, S. Túri, C. Baschirotto, N. Bresolin, Z. Vekerdy, Maria Teresa Bassi

Research output: Contribution to journalArticle

10 Citations (Scopus)
Original languageEnglish
Pages (from-to)591-593
Number of pages3
JournalClinical Genetics
Volume73
Issue number6
DOIs
Publication statusPublished - Jun 2008

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

First case of compound heterozygosity in ALS2 gene in infantile-onset ascending spastic paralysis with bulbar involvement. / Sztriha, L.; Panzeri, C.; Kálmánchey, R.; Szabó, R.; Endreffy, E.; Túri, S.; Baschirotto, C.; Bresolin, N.; Vekerdy, Z.; Bassi, Maria Teresa.

In: Clinical Genetics, Vol. 73, No. 6, 06.2008, p. 591-593.

Research output: Contribution to journalArticle

Sztriha, L. ; Panzeri, C. ; Kálmánchey, R. ; Szabó, R. ; Endreffy, E. ; Túri, S. ; Baschirotto, C. ; Bresolin, N. ; Vekerdy, Z. ; Bassi, Maria Teresa. / First case of compound heterozygosity in ALS2 gene in infantile-onset ascending spastic paralysis with bulbar involvement. In: Clinical Genetics. 2008 ; Vol. 73, No. 6. pp. 591-593.
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