DNA probes in Charcot-Marie-Tooth neuropathy.

Australian paediatric journal Pub Date : 1988-01-01
G A Nicholson, L R Griffiths, J G McLeod
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Abstract

Results of Duffy (Fy) linkage confirm genetic heterogeneity in Charcot-Marie-Tooth disease type 1 (CMT1). Of 11 families informative for Fy, four showed probable linkage with CMT1, seven showed-probable non-linkage and two showed definite non-linkage. These results suggest that Fy linked CMT1 may be less common than previously thought. These results combined with those of another DNA probe for the antithrombin III gene confirm that there are at least two gene loci for CMT1, termed 1A and 1B.

Charcot-Marie-Tooth神经病变的DNA探针。
Duffy (Fy)连锁结果证实了1型Charcot-Marie-Tooth病(CMT1)的遗传异质性。在11个具有Fy信息的家族中,4个与CMT1可能有连锁关系,7个可能无连锁关系,2个明确无连锁关系。这些结果表明,Fy相关的CMT1可能没有以前认为的那么常见。这些结果与抗凝血酶III基因的另一个DNA探针的结果相结合,证实CMT1至少有两个基因位点,称为1A和1B。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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