(Q34146843)

31 July 2017

0 references

A major locus for myoclonus-dystonia maps to chromosome 7q in eight families (English)

1 reference

31 July 2017

1 reference

S Frucht

13

1 reference

ORCID Public Data File 2021

Xandra O. Breakefield

5

object named as

X O Breakefield

1 reference

31 July 2017

C Klein

1

1 reference

31 July 2017

K Schilling

2

1 reference

31 July 2017

R J Saunders-Pullman

3

1 reference

31 July 2017

J Garrels

4

1 reference

31 July 2017

M F Brin

6

1 reference

31 July 2017

D deLeon

7

1 reference

31 July 2017

D Doheny

8

1 reference

31 July 2017

S Fahn

9

1 reference

31 July 2017

J S Fink

10

1 reference

31 July 2017

L Forsgren

11

1 reference

31 July 2017

J Friedman

12

1 reference

31 July 2017

J Harris

14

1 reference

31 July 2017

G Holmgren

15

1 reference

31 July 2017

B Kis

16

1 reference

31 July 2017

R Kurlan

17

1 reference

31 July 2017

M Kyllerman

18

1 reference

31 July 2017

A E Lang

19

1 reference

31 July 2017

J Leung

20

1 reference

31 July 2017

D Raymond

21

1 reference

31 July 2017

J D Robishaw

22

1 reference

31 July 2017

G Sanner

23

1 reference

31 July 2017

E Schwinger

24

1 reference

31 July 2017

R E Tabamo

25

1 reference

31 July 2017

M Tagliati

26

1 reference

31 July 2017

language of work or name

English

0 references

publication date

5 October 2000

1 reference

American Journal of Human Genetics

31 July 2017

1 reference

31 July 2017

67

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31 July 2017

5

1 reference

31 July 2017

1314-1319

1 reference

Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia.

31 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288573

Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288573

Association of a missense change in the D2 dopamine receptor with myoclonus dystonia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288573

A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288573

Essential myoclonus and myoclonic dystonia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288573

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288573

Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288573

D2 dopamine receptor gene in myoclonic dystonia and essential myoclonus

5 July 2018

1 reference

12 December 2020

Hereditary essential myoclonus

1 reference

12 December 2020

Myoclonus and dystonia: a family study

1 reference

12 December 2020

Classification of dystonia

1 reference

12 December 2020

Inherited myoclonus-dystonia syndrome

1 reference

12 December 2020

Alcohol-responsive myoclonic dystonia in a large family: dominant inheritance and phenotypic variation

1 reference

12 December 2020

Identifiers

DOI

10.1086/321193

1 reference

31 July 2017

1 reference

31 July 2017

1 reference