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Correlation between Pituitary Stalk Interruption Syndrome and Prokineticin Receptor 2 and Prokineticin 2 Mutations / 中国医学科学院学报
Acta Academiae Medicinae Sinicae ; (6): 37-41, 2016.
Article in English | WPRIM | ID: wpr-289909
ABSTRACT
<p><b>OBJECTIVE</b>To analyze the correlation between pituitary stalk interruption syndrome (PSIS) and prokineticin receptor 2 (PROKR2) and prokineticin 2 (RROK2) mutations.</p><p><b>METHODS</b>PROKR2 and RROK2 genotypes were identified by multiplex polymerase chain reaction analysis with exon-flanking primers and by automated sequencing techniques with peripheral blood DNA samples from 59 patients with PSIS.</p><p><b>RESULTS</b>Of these 59 PSIS patients, 6 showed intragenic deletions at the PROKR2 locus. Of them, 5 patients exhibited intragenic subsititution of exon 2 (c.991G>A), and the remaining one patient exhibited intragenic subsititution of exon 2 (c.1057C>T). No PROK2 mutation was found in these PSIS patients.</p><p><b>CONCLUSION</b>PROKR2 may be the susceptibility gene of PSIS.</p>
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pituitary Diseases / Neuropeptides / Exons / Receptors, Peptide / Receptors, G-Protein-Coupled / Gastrointestinal Hormones / Genotype / Mutation Limits: Humans Language: English Journal: Acta Academiae Medicinae Sinicae Year: 2016 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pituitary Diseases / Neuropeptides / Exons / Receptors, Peptide / Receptors, G-Protein-Coupled / Gastrointestinal Hormones / Genotype / Mutation Limits: Humans Language: English Journal: Acta Academiae Medicinae Sinicae Year: 2016 Type: Article