(Q34754070)

4 August 2017

Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy (English)

1 reference

4 August 2017

6

1 reference

4 August 2017

7

1 reference

4 August 2017

18

Rouleau GA

1 reference

ORCID Public Data File 2021

4 August 2017

1 reference

author name string

Minassian BA

1

1 reference

4 August 2017

Lee JR

2

1 reference

4 August 2017

Herbrick JA

3

1 reference

4 August 2017

Huizenga J

4

1 reference

4 August 2017

Soder S

5

1 reference

4 August 2017

Gardner R

8

1 reference

4 August 2017

Fong CY

9

1 reference

4 August 2017

Carpenter S

10

1 reference

4 August 2017

Jardim L

11

1 reference

4 August 2017

Satishchandra P

12

1 reference

4 August 2017

Andermann E

13

1 reference

4 August 2017

Snead OC 3rd

14

1 reference

4 August 2017

Lopes-Cendes I

15

1 reference

4 August 2017

Tsui LC

16

1 reference

4 August 2017

Delgado-Escueta AV

17

1 reference

4 August 2017

Scherer SW

19

1 reference

4 August 2017

language of work or name

English

0 references

publication date

1 October 1998

1 reference

4 August 2017

1 reference

4 August 2017

20

1 reference

4 August 2017

171-174

1 reference

4 August 2017

2

1 reference

https://scigraph.springernature.com/pub.10.1038/2470

4 August 2017

0 references

cites work

Progressive myoclonus epilepsies: specific causes and diagnosis

1 reference

21 January 2018

Complex febrile seizures

1 reference

Progressive familial myoclonic epilepsy in three families: its clinical features and pathological basis.

21 January 2018

1 reference

LAFORA'S DISEASE. DISTINCT CLINICO-PATHOLOGIC FORM OF UNVERRICHT'S SYNDROME.

21 January 2018

1 reference

Studies in myoclonus epilepsy (Lafora body form). II. Polyglucosans in the systemic deposits of myoclonus epilepsy and in corpora amylacea

21 January 2018

1 reference

Lafora's disease: peroxisomal storage in skeletal muscle.

21 January 2018

1 reference

The gene for progressive myoclonus epilepsy of the Lafora type maps to chromosome 6q.

21 January 2018

1 reference

Lafora progressive myoclonus epilepsy: narrowing the chromosome 6q24 locus by recombinations and homozygosities

21 January 2018

1 reference

Interpreting cDNA sequences: some insights from studies on translation

21 January 2018

1 reference

Crystal structure of the dual specificity protein phosphatase VHR

21 January 2018

1 reference

Form and function in protein dephosphorylation

21 January 2018

1 reference

A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast

21 January 2018

1 reference

Association of SET domain and myotubularin-related proteins modulates growth control

21 January 2018

1 reference

From form to function: signaling by protein tyrosine phosphatases.

21 January 2018

1 reference

Differential pre- and postsynaptic modulation of chemical transmission in the squid giant synapse by tyrosine phosphorylation

21 January 2018

1 reference

Lafora's disease in south India: a clinical, electrophysiologic, and pathologic study.

21 January 2018

1 reference

Sweat gland duct cells in Lafora disease: diagnosis by skin biopsy

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

The N-methyl-D-aspartate receptor subunits NR2A and NR2B bind to the SH2 domains of phospholipase C-gamma.

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/2470

1 reference

4 August 2017

1 reference