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Oligophrenin
LE WE PMID CA
Oligophrenin2036Oligophrenin

Amphiphysin

APPL1

APPL2

Arfaptin2

BAR protein domain

Endophilin

Oligophrenin

Sorting nexin

2003  
1
Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia.
[12805098] Brain 126(Pt 7): 1537-44 (2003)
2004  
2
The BAR-domain family of proteins: a case of bending and binding?
[14993925] EMBO Rep 5(3): 250-5 (2004)

Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth

All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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