(Q41434896)

English

Mutation watch

scientific article published on May 1997

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scholarly article

1 reference

Europe PubMed Central

30 September 2017

1 reference

Europe PubMed Central

Mutation watch (English)

1 reference

Europe PubMed Central

30 September 2017

author name string

Meisler M

1

1 reference

Europe PubMed Central

30 September 2017

publication date

1 May 1997

1 reference

Europe PubMed Central

30 September 2017

number of pages

2

1 reference

based on heuristic

inferred from page(s)

Mammalian Genome

1 reference

Europe PubMed Central

30 September 2017

8

1 reference

Europe PubMed Central

30 September 2017

5

1 reference

Europe PubMed Central

30 September 2017

305-306

1 reference

Europe PubMed Central

30 September 2017

https://scigraph.springernature.com/pub.10.1007/s003359900428

0 references

Cholesterol modification of hedgehog signaling proteins in animal development

1 reference

https://api.crossref.org/works/10.1007%2FS003359900428

21 January 2018

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function

1 reference

https://api.crossref.org/works/10.1007%2FS003359900428

21 January 2018

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.

1 reference

https://api.crossref.org/works/10.1007%2FS003359900428

21 January 2018

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

1 reference

https://api.crossref.org/works/10.1007%2FS003359900428

21 January 2018

Absence epilepsy in tottering mutant mice is associated with calcium channel defects

1 reference

https://api.crossref.org/works/10.1007%2FS003359900428

21 January 2018

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

1 reference

https://api.crossref.org/works/10.1007%2FS003359900428

21 January 2018

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

1 reference

https://api.crossref.org/works/10.1007%2FS003359900428

21 January 2018

Inner ear defects induced by null mutation of the isk gene

1 reference

https://api.crossref.org/works/10.1007%2FS003359900428

21 January 2018

Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice

1 reference

https://api.crossref.org/works/10.1007%2FS003359900428

21 January 2018

Identifiers

10.1007/S003359900428

1 reference

Europe PubMed Central

30 September 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

30 September 2017

ResearchGate publication ID

0 references

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