Mutations and deletions in PCDH19 account for various...

Human Mutation 2011 Vol. 32; Iss. 1

Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females

Christel Depienne, Oriane Trouillard, Delphine Bouteiller, Isabelle Gourfinkel-An, Karine Poirier, François Rivier, Patrick Berquin, Rima Nabbout, Denys Chaigne, Dominique Steschenko, Agnès Gautier, D
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Volume:
32
Year:
2011
Pages:
1
DOI:
10.1002/humu.21373
File:
PDF, 577 KB
2011
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