【発明の名称】小児脊髄性筋萎縮症の遺伝子座に連結したマーカーの検出方法およびプローブ - Anstitu National de la Sante et de la Lecherche Medical

Title:

【発明の名称】小児脊髄性筋萎縮症の遺伝子座に連結したマーカーの検出方法およびプローブ

Document Type and Number:

Japanese Patent JPH10500860

Kind Code:

A

Abstract:

PCT No. PCT/FR95/00722 Sec. 371 Date Jan. 29, 1997 Sec. 102(e) Date Jan. 29, 1997 PCT Filed Jun. 2, 1995 PCT Pub. No. WO95/33852 PCT Pub. Date Dec. 14, 1995The invention relates to methods and compositions for detecting the presence of genetic alterations in the human 5q13 chromosomal region. More specifically, the invention relates to nucleic acids, probes, primers, and methods of using the same, for the amplification and/or the detection of alterations in the human 5q13 chromosomal region, and their correlation to spinal muscular atrophy.

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Inventors:

Melchi, Judith
Munich, arnold

Application Number:

JP50045396A

Publication Date:

January 27, 1998

Filing Date:

June 02, 1995

Export Citation:

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Assignee:

Anstitu National de la Sante et de la Lecherche Medical

International Classes:

C07K14/475; C12N15/12; C12Q1/68; C12N15/09; C12Q1/6858; C12Q1/6876; C12Q1/6883; (IPC1-7): C12N15/09; C12Q1/68

Attorney, Agent or Firm:

Hajime Tsukuni (3 outside)

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