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A homozygous FKRP start codon mutation is associated with Walker–Warburg syndrome, the severe end of the clinical spectrum

✍ Scribed by J Van Reeuwijk; MJW Olderode-Berends; C Van Den Elzen; OF Brouwer; T Roscioli; MG Van Pampus; H Scheffer; HG Brunner; H Van Bokhoven; FA Hol


Book ID
110888997
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
705 KB
Volume
78
Category
Article
ISSN
0009-9163

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