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Article

A novel homozygous truncating mutation of the SFRP4 gene in Pyle's disease.

Clinical genetics - 1 Jul 2017

Chatron N, Lesca G, Labalme A, Rollat-Farnier P A, Monin P, Pichot E, Edery P, Sanlaville D, Rossi M

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Identifiers

PMID: 28090630
DOI: 10.1111/cge.12907

Genes

SFRP4

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