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Ryuko Murakami

Okayama University

4

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64

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A newly identified null allelic mutation in the human lipoprotein lipase (LPL) gene of a compound heterozygote with familial LPL deficiency

1992 Biochimica et Biophysica Acta
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Terminal 22q deletion associated with a partial deficiency of arylsulphatase A.

1992 Journal of Medical Genetics
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Unique karyotypes in two patients with Prader‐Willi syndrome

1992 American Journal of Medical Genetics
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