Article
Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndrome.
Cytogenetics and cell genetics - 1 Jan 2001
Marneros A G, Mehenni H, Reichenberger E, Antonarakis S E, Krieg T, Olsen B R
Abstract excerpt
Mutations in the serine/threonine kinase STK11 lead to Peutz-Jeghers syndrome (PJS) in a subset of affected individuals. Significant evidence for linkage to a second potential PJS disease locus on 19q13.4 has previously been described in one PJS family (PJS07). In the current study, we investigat...
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