(Q24311730)

GOA release 2020-03-11

1 reference

D Vetrie

13

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author name string

H Jin

1

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M May

2

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L Tranebjaerg

3

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E Kendall

4

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G Fontán

5

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J Jackson

6

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S H Subramony

7

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F Arena

8

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H Lubs

9

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S Smith

10

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R Stevenson

11

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C Schwartz

https://scigraph.springernature.com/pub.10.1038/ng1096-177

12

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language of work or name

English

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publication date

October 1996

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published in

Nature Genetics

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volume

14

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page(s)

177-80

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issue

2

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exact match

0 references

cites work

Isolation of cosmid and cDNA clones in the region surrounding the BTK gene at Xq21.3-q22

1 reference

https://api.crossref.org/works/10.1038/NG1096-177

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

BTKbase, mutation database for X-linked agammaglobulinemia (XLA).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

Construction of a 5.2-megabase physical map of the human X chromosome at Xq22 using pulsed-field gel electrophoresis and yeast artificial chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

A 6.5-Mb yeast artificial chromosome contig incorporating 33 DNA markers on the human X chromosome at Xq22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

Physical mapping of DNA markers in the q13-q22 region of the human X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

Familial spastic paraparesis and deafness. A new x-linked neurodegenerative disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

Infantile X-linked ataxia and deafness: a new clinicopathologic entity?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

Huntington's disease gene (IT15) is widely expressed in human and rat tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

7 January 2021

Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

7 January 2021

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

7 January 2021

Familial opticoacoustic nerve degeneration and polyneuropathy

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

7 January 2021

Nerve deafness: optic nerve atrophy, and dementia: a new X-linked recessive syndrome?

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

7 January 2021

A new X-linked syndrome comprising progressive basal ganglion dysfunction, mental and growth retardation, external ophthalmoplegia, postnatal microcephaly and deafness

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

7 January 2021

X-linked ataxia, weakness, deafness, and loss of vision in early childhood with a fatal course.

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

7 January 2021

Identification of Btk mutations in 20 unrelated patients with X-Iinked agammaglobulinaemia (XLA)

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

7 January 2021

Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR.

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-177

7 January 2021