Spectrum of Mutations in the Batten Disease Gene, CLN3-Reference-Cited by-同舟云学术

Spectrum of Mutations in the Batten Disease Gene, CLN3

Published:1997-08 Issue:2 Volume:61 Page:310-316
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Munroe Patricia B.,Mitchison Hannah M.,O'Rawe Angela M.,Anderson John W.,Boustany Rose-Mary,Lerner Terry J.,Taschner Peter E.M.,Vos Nanneke de,Breuning Martijn H.,Gardiner R. Mark,Mole Sara E.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference22 articles.

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2. Antonarakis SE (1996) Recommendations for a nomenclature system for human gene mutations (http://ariel.ucs.unimelb.edu.au:80/∼cotton/antonara.htm)

3. Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12;Callen;Am J Hum Genet,1991

4. Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients;Dean;Cell,1990

5. Batten disease (Spielmeyer-Sjögren disease) and haptoglobins (HP): indication of linkage and assignment to chromosome 16;Eiberg;Clin Genet,1989

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