Trinucleotide expansion diseases in the context of micro- and minisatellite evolution, Hammersmith Hospital, April 1-3, 1998.

The EMBO journal ·Vol. 17 ·No. 19 ·1998-10-01 ·Pages 5521-4

Hancock JM, Santibáñez-Koref MF

Abstract

暂无摘要

MeSH Terms

Chromosome Aberrations Chromosome Disorders Evolution, Molecular Fragile X Syndrome/genetics Humans Muscular Atrophy/genetics Mutagenesis Myotonic Dystrophy/genetics Trinucleotide Repeat Expansion

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Hancock J M

Comparative Sequence Analysis Group, MRC Clinical Sciences Centre, Hammersmith Hospital, London W12 0NN, UK.

Santibáñez-Koref M F

References (2)

2 references, click to expand

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.
Nature. 1991 Jul 4;352(6330):77-9 PMID: 2062380
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.
Science. 1991 Jun 21;252(5013):1711-4 PMID: 1675488

Article Info

Journal

The EMBO journal

Abbr.

EMBO J

ISSN

0261-4189

DOI

10.1093/emboj/17.19.5521

Published

1998-10-01

Pages

5521-4

Language

English

Region

England

NLM ID

8208664

PMCID

PMC1170879

Subset

External Links

PubMed source DOI: 10.1093/emboj/17.19.5521 PMC Full Text View journal details

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Trinucleotide expansion diseases in the context of micro- and minisatellite evolution, Hammersmith Hospital, April 1-3, 1998.

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