A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrum. (Q48270083)
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scientific article published on 11 February 2010
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrum. |
scientific article published on 11 February 2010 |
Statements
A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrum (English)
J Van Reeuwijk
M J W Olderode-Berends
C Van den Elzen
O F Brouwer
T Roscioli
M G Van Pampus
H G Brunner
11 February 2010
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