Schopf-Schulz-Passarge syndrome resulting from a recurrent homozygous nonsense mutation, p.Cys107X, in WNT10A

Research output: Contribution to journal › Meeting abstract

Original language	English
Pages (from-to)	931 - 931
Number of pages	1
Journal	British Journal of Dermatology
Volume	164
Issue number	4
Publication status	Published - 2011

Cite this

@article{eab1c4190d3d403f956aab6d972f7752,

title = "Schopf-Schulz-Passarge syndrome resulting from a recurrent homozygous nonsense mutation, p.Cys107X, in WNT10A",

author = "G. Petrof and K. Fong and Lai-Cheong, {J. E.} and Cockayne, {S. E.} and McGrath, {J. A.}",

year = "2011",

language = "English",

volume = "164",

pages = "931 -- 931",

journal = "British Journal of Dermatology",

issn = "1365-2133",

publisher = "John Wiley & Sons, Ltd (10.1111)",

number = "4",

}

TY - JOUR

T1 - Schopf-Schulz-Passarge syndrome resulting from a recurrent homozygous nonsense mutation, p.Cys107X, in WNT10A

AU - Petrof, G.

AU - Fong, K.

AU - Lai-Cheong, J. E.

AU - Cockayne, S. E.

AU - McGrath, J. A.

PY - 2011

Y1 - 2011

M3 - Meeting abstract

SN - 1365-2133

VL - 164

SP - 931

EP - 931

JO - British Journal of Dermatology

JF - British Journal of Dermatology

IS - 4

ER -