The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy (Q24308680)

NLR family apoptosis inhibitory protein

inferred from title

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nervous system development

GOA release 2020-03-11

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GOA release 2020-03-11

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N Roy

1

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M S Mahadevan

2

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M McLean

3

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G Shutler

4

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Z Yaraghi

5

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R Farahani

6

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S Baird

7

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A Besner-Johnston

8

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C Lefebvre

9

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X Kang

Fine mapping and narrowing of the genetic interval of the spinal muscular atrophy region by linkage studies

10

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publication date

13 January 1995

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language of work or name

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80

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issue

1

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page(s)

167-78

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cites work

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The Human γ-Aminobutyric Acid Receptor Subunit β3 and α5 Gene Cluster in Chromosome 15q11-q13 Is Rich in Highly Polymorphic (CA)n Repeats

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Large linkage analysis in 100 families with autosomal recessive spinal muscular atrophy (SMA) and 11 CEPH families using 15 polymorphic loci in the region 5q11.2-q13.3.

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A multicopy dinucleotide marker that maps close to the spinal muscular atrophy gene.

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Mapping of two new markers within the smallest interval harboring the spinal muscular atrophy locus by family and radiation hybrid analysis

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Linkage mapping of the spinal muscular atrophy gene

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Genetic linkage analysis of Canadian spinal muscular atrophy kindreds using flanking microsatellite 5q13 polymorphisms

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Steroid 21-hydroxylase (P450c21): a new allele and spread of mutations through the pseudogene

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Is Werdnig-Hoffmann disease a pure lower motor neuron disorder?

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Identification and characterization of a spinal muscular atrophy-determining gene

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Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia

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Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6.

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Refined physical map of the spinal muscular atrophy gene (SMA) region at 5q13 based on YAC and cosmid contiguous arrays.

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Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q

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Genetic homogeneity between acute and chronic forms of spinal muscular atrophy

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A de novo pathological point mutation at the 21-hydroxylase locus: implications for gene conversion in the human genome

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High resolution physical map of the region surrounding the spinal muscular atrophy gene

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Two 5q13 simple tandem repeat loci are in linkage disequilibrium with type 1 spinal muscular atrophy.

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An apoptosis-inhibiting baculovirus gene with a zinc finger-like motif

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Cell death during development of the nervous system

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