Isolation of a novel gene mutated in Wiskott-Aldrich syndrome.

Derry, J M; Ochs, H D; Francke, U

Derry, J M; Ochs, H D; Francke, U.

Affiliation

Derry JM; Howard Hughes Medical Institute, Beckman Center for Molecular and Genetic Medicine, Stanford, California.

Cell ; 78(4): 635-44, 1994 Aug 26.

Article in En | MEDLINE | ID: mdl-8069912

Subject(s)

Proteins/genetics; Wiskott-Aldrich Syndrome/genetics; X Chromosome; Amino Acid Sequence; Amino Acids/analysis; Base Sequence; Chromosome Mapping; Cloning, Molecular; DNA, Complementary/genetics; Female; Genetic Linkage; Humans; Infant; Male; Molecular Sequence Data; Organ Specificity; Pedigree; Point Mutation/genetics; RNA, Messenger/analysis; Sequence Analysis, DNA; Sequence Deletion/genetics; Wiskott-Aldrich Syndrome Protein

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Wiskott-Aldrich Syndrome / X Chromosome / Proteins Limits: Female / Humans / Infant / Male Language: En Journal: Cell Year: 1994 Document type: Article Country of publication: United States

Search on Google

Add to My VHL

XML

PubMed Links