PARTIAL DELETIONS OF PUTATIVE ADRENOLEUKODYSTROPHY (ALD) GENE IN JAPANESE ALD PATIENTS

被引：10

作者：

KOIKE, R

ONODERA, O

TABE, H

KANEKO, K

MIYATAKE, T

IWASAKI, S

NAKANO, M

SHIZUMA, N

IKEGUCHI, K

NISHIZAWA, M

MOSSER, J

SARDE, CO

TSUJI, S

机构：

[1] TOKYO MED & DENT UNIV,DEPT NEUROL,TOKYO 113,JAPAN

[2] SAITAMA MED SCH,DEPT NEUROL,MOROYAMA,SAITAMA 35004,JAPAN

[3] OSAKA UNIV,DEPT NEUROL,OSAKA,JAPAN

[4] JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN

[5] FAC MED STRASBOURG,INST CHIM BIOL,CNRS,GENET MOLEC EUCARYOTES LAB,INSERM,UNITE 184,F-67085 STRASBOURG,FRANCE

来源：

HUMAN MUTATION | 1995年 / 6卷 / 03期

关键词：

D O I：

10.1002/humu.1380060314

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：263 / 267

页数：5

共 18 条

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[2]

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[5]

FEIL R, 1991, AM J HUM GENET, V49, P1361

[6] ADRENOMYELONEUROPATHY - PROBABLE VARIANT OF ADRENOLEUKODYSTROPHY .1. CLINICAL AND ENDOCRINOLOGIC ASPECTS [J].

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NEUROLOGY, 1977, 27 (12) :1107-1113

[7]

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[8]

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[9] ADRENOLEUKOMYELONEUROPATHY PRESENTING AS SPINOCEREBELLAR DEGENERATION [J].

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[10]

MGEON BR, 1981, P NATL ACAD SCI USA, V78, P5066

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