(Q34380159)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15621877%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

title

Mutation analysis of the KIF21A gene in an Indian family with CFEOM1: implication of CpG methylation for most frequent mutations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15621877%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

0 references

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15621877%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

author name string

Conjeevaram Venkatesh

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15621877%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

Anitha Ragunath

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15621877%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

Arun Kumar

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15621877%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

publication date

1 December 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15621877%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15621877%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

volume

25

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15621877%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15621877%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

page(s)

247-255

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15621877%20AND%20SRC:MED&resulttype=core&format=json

Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2

6 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1080%2F13816810490498198

All kinesin superfamily protein, KIF, genes in mouse and human

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490498198

The CpG dinucleotide and human genetic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490498198

Paternal origin of new mutations in von Recklinghausen neurofibromatosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490498198

Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490498198

10.1080/13816810490498198

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15621877%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

1 reference