PAK3 mutation in nonsyndromic X-linked mental retardation.

Allen, K M; Gleeson, J G; Bagrodia, S; Partington, M W; MacMillan, J C; Cerione, R A; Mulley, J C; Walsh, C A

Allen, K M; Gleeson, J G; Bagrodia, S; Partington, M W; MacMillan, J C; Cerione, R A; Mulley, J C; Walsh, C A.

Affiliation

Allen KM; Division of Neurogenetics, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02115, USA.

Nat Genet ; 20(1): 25-30, 1998 Sep.

Article in En | MEDLINE | ID: mdl-9731525

Subject(s)

Brain/metabolism; Intellectual Disability/genetics; Mutation; Protein Serine-Threonine Kinases/genetics; X Chromosome; Animals; Base Sequence; COS Cells; Cloning, Molecular; Female; Fluorescent Antibody Technique, Indirect; Humans; Male; Mice; Molecular Sequence Data; Pedigree; Protein Serine-Threonine Kinases/metabolism; Rats; Recombinant Proteins/genetics; Recombinant Proteins/metabolism; Sequence Analysis, DNA; p21-Activated Kinases

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Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Brain / Protein Serine-Threonine Kinases / Intellectual Disability / Mutation Limits: Animals / Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 1998 Document type: Article Affiliation country: United States

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