(Q28295300)

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Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndrome

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title

Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndrome (English)

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main subject

Prader–Willi syndrome

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5

Karin Buiting

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Denise Horn

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3

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Denise Horn

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author name string

Maren Runte

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1

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Raymonda Varon

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2

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Bernhard Horsthemke

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4

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language of work or name

English

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publication date

February 2005

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published in

Human Genetics

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volume

116

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page(s)

228-30

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issue

3

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exact match

https://scigraph.springernature.com/pub.10.1007/s00439-004-1219-2

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cites work

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565282

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Familial interstitial 570 kbp deletion of theUBE3Agene region causing Angelman syndrome but not Prader-Willi syndrome

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565282

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patient.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565282

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12 December 2020

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Epilepsy and obesity in serotonin 5-HT2C receptor mutant mice

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https://pubmed.ncbi.nlm.nih.gov/15565282

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12 December 2020

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DNA deletion and its parental origin in Angelman syndrome patients

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565282

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12 December 2020

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Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndrome

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15565282

retrieved

12 December 2020

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Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565282

retrieved

12 December 2020

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(Q28295300)

Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndrome

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