Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresis.

A. van der Zwaag; J.P.H. Burbach; H.G. Brunner; H. van Bokhoven; G.W. Padberg

Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresis.

Translated title of the contribution: Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresis.

A. van der Zwaag, J.P.H. Burbach, H.G. Brunner, H. van Bokhoven, G.W. Padberg

Translational Neuroscience

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

Translated title of the contribution	Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresis.
Original language	Undefined/Unknown
Pages (from-to)	66-71
Number of pages	6
Journal	Developmental Brain Research
Volume	158
Issue number	1-2
Publication status	Published - 2005

Cite this

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title = "Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresis.",

author = "{van der Zwaag}, A. and J.P.H. Burbach and H.G. Brunner and {van Bokhoven}, H. and G.W. Padberg",

year = "2005",

language = "Undefined/Unknown",

volume = "158",

pages = "66--71",

journal = "Developmental Brain Research",

issn = "0165-3806",

publisher = "Elsevier",

number = "1-2",

}

TY - JOUR

T1 - Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresis.

AU - van der Zwaag, A.

AU - Burbach, J.P.H.

AU - Brunner, H.G.

AU - van Bokhoven, H.

AU - Padberg, G.W.

PY - 2005

Y1 - 2005

M3 - Article

SN - 0165-3806

VL - 158

SP - 66

EP - 71

JO - Developmental Brain Research

JF - Developmental Brain Research

IS - 1-2

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