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Gene screening in five Chinese families with hereditary spastic paraplegia with thin corpus callosum / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 677-680, 2007.
Article in Chinese | WPRIM | ID: wpr-229846
ABSTRACT
<p><b>OBJECTIVE</b>To screen all ten genes between D15S971 and D15S1012 in five Chinese families with hereditary spastic paraplegia with thin corpus callosum (HSP-TCC).</p><p><b>METHODS</b>DNA samples from 5 HSP-TCC families were screened for mutations in AK128197, MGC14798, HH114, MEIS2, MGC35118, SPRED1, AK128458, FLJ38426, RASGRP1 and AK093014 on chromosome 15q13-15 between microsatellites D15S971 and D15S1012 by polymerase chain reaction, direct sequencing and cosegreagation analysis.</p><p><b>RESULTS</b>No disease-causing mutations were found in the 10 genes, but 13 polymorphisms were identified in which two were novel.</p><p><b>CONCLUSION</b>This study did not support the ten genes between D15S971 and D15S1012 were the disease-causing genes of the 5 HSP-TCC families.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Chromosomes, Human, Pair 15 / Spastic Paraplegia, Hereditary / Corpus Callosum / Paraparesis, Spastic / Asian People / Genes, Recessive / Genetics Type of study: Diagnostic study / Screening study Limits: Adult / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2007 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Chromosomes, Human, Pair 15 / Spastic Paraplegia, Hereditary / Corpus Callosum / Paraparesis, Spastic / Asian People / Genes, Recessive / Genetics Type of study: Diagnostic study / Screening study Limits: Adult / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2007 Type: Article