High incidence of spinal muscular atrophy type I (Werdnig - Hoffmann disease) in the Karaite community in Israel (Q67693745)

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scientific article published on 01 October 1977

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Language	Label	Description	Also known as
English	High incidence of spinal muscular atrophy type I (Werdnig - Hoffmann disease) in the Karaite community in Israel	scientific article published on 01 October 1977

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

912942

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:912942%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 September 2019

title

High incidence of spinal muscular atrophy type I (Werdnig - Hoffmann disease) in the Karaite community in Israel (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

912942

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:912942%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 September 2019

main subject

spinal muscular atrophy

1 reference

based on heuristic

inferred from title

muscular atrophy

1 reference

based on heuristic

inferred from title

author name string

K. Fried

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

912942

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A912942

retrieved

6 August 2022

G. Mundel

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

912942

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A912942

retrieved

6 August 2022

language of work or name

English

1 reference

stated in

National Center for Biotechnology Information

PubMed publication ID

912942

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=912942

retrieved

6 August 2022

publication date

1 October 1977

1 reference

stated in

Europe PubMed Central

PubMed publication ID

912942

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:912942%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 September 2019

published in

Clinical Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

912942

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:912942%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 September 2019

volume

12

1 reference

stated in

Europe PubMed Central

PubMed publication ID

912942

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:912942%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 September 2019

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

912942

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:912942%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 September 2019

page(s)

250-251

1 reference

stated in

Europe PubMed Central

PubMed publication ID

912942

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:912942%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 September 2019

Identifiers

DOI

10.1111/J.1399-0004.1977.TB00934.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

912942

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:912942%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 September 2019

PubMed publication ID

912942

1 reference

stated in

Europe PubMed Central

PubMed publication ID

912942

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:912942%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 September 2019

 

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