(Q40629467)

22 September 2017

Two sibs with myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders (English)

1 reference

22 September 2017

0 references

1 reference

1 reference

Mégarbané A

1

1 reference

22 September 2017

Khalil G

2

1 reference

22 September 2017

Waked N

3

1 reference

22 September 2017

Rötig A

4

1 reference

22 September 2017

Caillaud C

5

1 reference

22 September 2017

Loiselet J

6

1 reference

22 September 2017

language of work or name

1 reference

1 December 1999

1 reference

American Journal of Medical Genetics Part A

22 September 2017

1 reference

22 September 2017

87

1 reference

22 September 2017

4

1 reference

22 September 2017

289-293

1 reference

Premature atherosclerosis with photomyoclonic epilepsy, deafness, diabetes mellitus, nephropathy, and neurodegenerative disorder in two brothers: a new syndrome?

22 September 2017

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991203%2987%3A4%3C289%3A%3AAID-AJMG1%3E3.0.CO%3B2-T

Crossref

reference URL

HEREDITARY PHOTOMYOCLONUS ASSOCIATED WITH DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRAL DYSFUNCTION.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991203%2987%3A4%3C289%3A%3AAID-AJMG1%3E3.0.CO%3B2-T

Crossref

reference URL

Familial myoclonus, cerebellar ataxia, and deafness. Specific genetically-determined disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991203%2987%3A4%3C289%3A%3AAID-AJMG1%3E3.0.CO%3B2-T

Crossref

reference URL

10.1002/(SICI)1096-8628(19991203)87:4<289::AID-AJMG1>3.0.CO;2-T

21 January 2018

Identifiers

DOI

1 reference

22 September 2017

1 reference