What does the nature of the MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome?

J. Zhang, X. Bao, G. Cao, S. Jiang, X. Zhu, H. Lu, L. Jia, H. Pan, S. Fehr, M. Davis, Helen Leonard, David Ravine, X. Wu

Research output: Contribution to journalArticle

6 Citations (Scopus)
Original languageEnglish
Pages (from-to)526-533
JournalClinical Genetics
Volume82
Issue number6
DOIs
Publication statusPublished - 2012

Cite this

Zhang, J. ; Bao, X. ; Cao, G. ; Jiang, S. ; Zhu, X. ; Lu, H. ; Jia, L. ; Pan, H. ; Fehr, S. ; Davis, M. ; Leonard, Helen ; Ravine, David ; Wu, X. / What does the nature of the MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome?. In: Clinical Genetics. 2012 ; Vol. 82, No. 6. pp. 526-533.
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title = "What does the nature of the MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome?",
author = "J. Zhang and X. Bao and G. Cao and S. Jiang and X. Zhu and H. Lu and L. Jia and H. Pan and S. Fehr and M. Davis and Helen Leonard and David Ravine and X. Wu",
year = "2012",
doi = "10.1111/j.1399-0004.2011.01838.x",
language = "English",
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pages = "526--533",
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Zhang, J, Bao, X, Cao, G, Jiang, S, Zhu, X, Lu, H, Jia, L, Pan, H, Fehr, S, Davis, M, Leonard, H, Ravine, D & Wu, X 2012, 'What does the nature of the MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome?' Clinical Genetics, vol. 82, no. 6, pp. 526-533. https://doi.org/10.1111/j.1399-0004.2011.01838.x

What does the nature of the MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome? / Zhang, J.; Bao, X.; Cao, G.; Jiang, S.; Zhu, X.; Lu, H.; Jia, L.; Pan, H.; Fehr, S.; Davis, M.; Leonard, Helen; Ravine, David; Wu, X.

In: Clinical Genetics, Vol. 82, No. 6, 2012, p. 526-533.

Research output: Contribution to journalArticle

TY - JOUR

T1 - What does the nature of the MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome?

AU - Zhang, J.

AU - Bao, X.

AU - Cao, G.

AU - Jiang, S.

AU - Zhu, X.

AU - Lu, H.

AU - Jia, L.

AU - Pan, H.

AU - Fehr, S.

AU - Davis, M.

AU - Leonard, Helen

AU - Ravine, David

AU - Wu, X.

PY - 2012

Y1 - 2012

U2 - 10.1111/j.1399-0004.2011.01838.x

DO - 10.1111/j.1399-0004.2011.01838.x

M3 - Article

VL - 82

SP - 526

EP - 533

JO - Clinical Genetics

JF - Clinical Genetics

SN - 0009-9163

IS - 6

ER -