(Q58152648)

1

object named as

Philippe Corcia

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author name string

Véronique Mayeux-Portas

2

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Jawad Khoris

3

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Alain Autret

5

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Jean-Pierre Müh

6

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William Camu

7

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Christian Andres

8

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the French ALS Research Group

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

9

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publication date

31 January 2002

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published in

Annals of Neurology

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volume

51

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issue

2

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page(s)

243-246

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cites work

1 reference

Identification and characterization of a spinal muscular atrophy-determining gene

21 January 2018

1 reference

Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene.

21 January 2018

1 reference

Deletions causing spinal muscular atrophy do not predispose to amyotrophic lateral sclerosis

21 January 2018

1 reference

Apolipoprotein E genotyping in sporadic amyotrophic lateral sclerosis: evidence for a major influence on the clinical presentation and prognosis.

21 January 2018

1 reference

Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number

21 January 2018

1 reference

Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

21 January 2018

1 reference

Genotype determination at the survival motor neuron locus in a normal population and SMA carriers using competitive PCR and primer extension

21 January 2018

1 reference

Sequence of a 131-kb region of 5q13.1 containing the spinal muscular atrophy candidate genes SMN and NAIP.

21 January 2018

1 reference

Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis

21 January 2018

1 reference

Analysis of chromosome 5q13 genes in amyotrophic lateral sclerosis: Homozygous naip deletion in a sporadic case

21 January 2018

1 reference