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

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

author = "L. Sztriha and C. Panzeri and R. K{\'a}lm{\'a}nchey and R. Szab{\'o} and E. Endreffy and S. T{\'u}ri and C. Baschirotto and N. Bresolin and Z. Vekerdy and Bassi, {Maria Teresa}",

year = "2008",

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doi = "10.1111/j.1399-0004.2008.00993.x",

language = "English",

volume = "73",

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T1 - First case of compound heterozygosity in ALS2 gene in infantile-onset ascending spastic paralysis with bulbar involvement

AU - Sztriha, L.

AU - Panzeri, C.

AU - Kálmánchey, R.

AU - Szabó, R.

AU - Endreffy, E.

AU - Túri, S.

AU - Baschirotto, C.

AU - Bresolin, N.

AU - Vekerdy, Z.

AU - Bassi, Maria Teresa

PY - 2008/6

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DO - 10.1111/j.1399-0004.2008.00993.x

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AN - SCOPUS:43449124426

VL - 73

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JO - Clinical Genetics

JF - Clinical Genetics

SN - 0009-9163

IS - 6

ER -

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

ASJC Scopus subject areas

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