(Q44231314)

English

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

scientific article published in September 1968

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

cerebellar ataxia

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

May DL

1

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

White HH

2

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

publication date

1 September 1968

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

Archives of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

19

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

331-338

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

Identifiers

10.1001/ARCHNEUR.1968.00480030109013

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 December 2017

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