Novel mutation and the first prenatal screening of cathepsin D deficiency (CLN10).
Fritchie K; Siintola E; Armao D; Lehesjoki AE; Marino T; Powell C; Tennison M; Booker JM; Koch S; Partanen S; Suzuki K; Tyynelä J; Thorne LB; Acta Neuropathologica, 2009, vol. 117, issue 2, p 201, ISSN 14320533. ISBN 14320533.

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