Additional Copies of the Proteolipid Protein Gene Causing Pelizaeus-Merzbacher Disease Arise by Separate Integration into the X Chromosome-Reference-Cited by-同舟云学术

Additional Copies of the Proteolipid Protein Gene Causing Pelizaeus-Merzbacher Disease Arise by Separate Integration into the X Chromosome

Published:2000-07 Issue:1 Volume:67 Page:14-22
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Hodes M.E.,Woodward Karen,Spinner Nancy B.,Emanuel Beverly S.,Enrico-Simon Agnes,Kamholz John,Stambolian Dwight,Zackai Elaine H.,Pratt Victoria M.,Thomas I.T.,Crandall Kerry,Dlouhy Stephen R.,Malcolm Sue

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference32 articles.

1. Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1A;Chance;Neurology,1992

2. An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region;Cremers;Hum Genet,1987

3. Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease;Ellis;Nat Genet,1994

4. From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins;Harding;Brain,1995

5. A case of Pelizaeus-Merzbacher disease showing increased dosage of the proteolipid protein gene;Harding;Neuropathol Appl Neurobiol,1995

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