Abstract:
:We have studied one family of a pedigree in which bulbospinal muscular atrophy and protanopia were segregated. Genotypes for these disorders were obtained on three generations, and the maximum likelihood estimate of recombination fraction was 0.4 with the lod score method. The results indicated that the two loci are not close; the locus for bulbospinal muscular atrophy is not located near the end of the long arm of the X chromosome.
journal_name
Neurologyjournal_title
Neurologyauthors
Mukai E,Yasuma Tdoi
10.1212/wnl.37.6.1019subject
Has Abstractpub_date
1987-06-01 00:00:00pages
1019-21issue
6eissn
0028-3878issn
1526-632Xjournal_volume
37pub_type
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