Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features-Reference-Cited by-同舟云学术

Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features

Published:2019-05-03 Issue:1 Volume:10 Page:
ISSN:2040-2392
Container-title:Molecular Autism
language:en
Short-container-title:Molecular Autism

Author:

Baker Emma K.^ORCID,Arpone Marta,Aliaga Solange M.,Bretherton Lesley,Kraan Claudine M.,Bui Minh,Slater Howard R.,Ling Ling,Francis David,Hunter Matthew F.,Elliott Justine,Rogers Carolyn,Field Michael,Cohen Jonathan,Cornish Kim,Santa Maria Lorena,Faundes Victor,Curotto Bianca,Morales Paulina,Trigo Cesar,Salas Isabel,Alliende Angelica M.,Amor David J.,Godler David E.

Publisher

Springer Science and Business Media LLC

Subject

Psychiatry and Mental health,Developmental Biology,Developmental Neuroscience,Molecular Biology

Link

http://link.springer.com/content/pdf/10.1186/s13229-019-0271-7.pdf

Reference63 articles.

1. Verkerk AJ, Pieretti M, Sutcliffe JS, Fu YH, Kuhl DP, Pizzuti A, et al. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell. 1991;65(5):905–14.

2. Kraan CM, Godler DE, Amor DJ. Epigenetics of fragile X syndrome and fragile X-related disorders. Dev Med Child Neurol. 2019;61(2):121–7.

3. Harris SW, Hessl D, Goodlin-Jones B, Ferranti J, Bacalman S, Barbato I, et al. Autism profiles of males with fragile X syndrome. Am J Ment Retard. 2008;113(6):427–38.

4. Rodriguez-Revenga L, Madrigal I, Badenas C, Xuncla M, Jimenez L, Mila M. Premature ovarian failure and fragile X female premutation carriers: no evidence for a skewed X-chromosome inactivation pattern. Menopause. 2009;16(5):944–9.

5. Sherman SL. Premature ovarian failure in the fragile X syndrome. Am J Med Genet. 2000;97(3):189–94.

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