Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia

N. Philip; B. Chabrol; A. M. Lossi; C. Cardoso; R. Guerrini; W. B. Dobyns; C. Raybaud; L. Villard

doi:10.1136/jmg.40.6.441

Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia

N. Philip, B. Chabrol, A. M. Lossi, C. Cardoso, R. Guerrini, W. B. Dobyns, C. Raybaud, L. Villard

Research output: Contribution to journal › Article › peer-review

Original language	English (US)
Pages (from-to)	441-446
Number of pages	6
Journal	Journal of medical genetics
Volume	40
Issue number	6
DOIs	https://doi.org/10.1136/jmg.40.6.441
State	Published - Jun 1 2003
Externally published	Yes

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10.1136/jmg.40.6.441

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@article{9a3852889c6642b09fae07f65db1fd69,

title = "Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia",

author = "N. Philip and B. Chabrol and Lossi, {A. M.} and C. Cardoso and R. Guerrini and Dobyns, {W. B.} and C. Raybaud and L. Villard",

year = "2003",

month = jun,

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doi = "10.1136/jmg.40.6.441",

language = "English (US)",

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AU - Guerrini, R.

AU - Dobyns, W. B.

AU - Raybaud, C.

AU - Villard, L.

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M3 - Article

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AN - SCOPUS:0037531657

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JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

SN - 0022-2593

IS - 6

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Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia

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