PAK3 related mental disability: Further characterization of the phenotype-Reference-Cited by-同舟云学术

PAK3 related mental disability: Further characterization of the phenotype

Published:2007 Issue:20 Volume:143A Page:2406-2416
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Peippo Maarit,Koivisto Anne M.,Särkämö Teppo,Sipponen Marjatta,von Koskull Harriet,Ylisaukko-oja Tero,Rehnström Karola,Froyen Guy,Ignatius Jaakko,Järvelä Irma

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.31956/fullpdf

Reference19 articles.

1. PAK3 mutation in nonsyndromic X-linked mental retardation

2. , . 2002. Bichemistry. New York: W.H. Freeman and Company. p 45–47.

3. Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation

4. The Mental Retardation Protein PAK3 Contributes to Synapse Formation and Plasticity in Hippocampus

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