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

doi:10.1111/j.1399-0004.2008.00993.x

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 journal › Article › peer-review

Original language	English
Pages (from-to)	591-593
Number of pages	3
Journal	Clinical Genetics
Volume	73
Issue number	6
DOIs	https://doi.org/10.1111/j.1399-0004.2008.00993.x
Publication status	Published - Jun 2008

ASJC Scopus subject areas

Genetics(clinical)
Genetics

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10.1111/j.1399-0004.2008.00993.x

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 journal › Article › peer-review

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