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A benigin allelic form of laminin alpha 2 chain deficient muscular dystrophy
被引:17
作者
:
Hayashi, YK
论文数:
0
引用数:
0
h-index:
0
机构:
NATL CTR NEUROL & PSYCHIAT,NATL INST NEUROSCI,DEPT NEUROMUSCULAR RES,KODAIRA,TOKYO 187,JAPAN
Hayashi, YK
Ishihara, T
论文数:
0
引用数:
0
h-index:
0
机构:
NATL CTR NEUROL & PSYCHIAT,NATL INST NEUROSCI,DEPT NEUROMUSCULAR RES,KODAIRA,TOKYO 187,JAPAN
Ishihara, T
Domen, K
论文数:
0
引用数:
0
h-index:
0
机构:
NATL CTR NEUROL & PSYCHIAT,NATL INST NEUROSCI,DEPT NEUROMUSCULAR RES,KODAIRA,TOKYO 187,JAPAN
Domen, K
论文数:
引用数:
h-index:
机构:
Hori, H
Arahata, K
论文数:
0
引用数:
0
h-index:
0
机构:
NATL CTR NEUROL & PSYCHIAT,NATL INST NEUROSCI,DEPT NEUROMUSCULAR RES,KODAIRA,TOKYO 187,JAPAN
Arahata, K
机构
:
[1]
NATL CTR NEUROL & PSYCHIAT,NATL INST NEUROSCI,DEPT NEUROMUSCULAR RES,KODAIRA,TOKYO 187,JAPAN
[2]
NATL HIGASHI SAITAMA HOSP,SAITAMA,JAPAN
[3]
SAITAMA REHABIL CTR,SAITAMA,JAPAN
[4]
TOKYO MED & DENT UNIV,MED RES INST,DEPT TISSUE PHYSIOL,TOKYO,JAPAN
来源
:
LANCET
|
1997年
/ 349卷
/ 9059期
关键词
:
D O I
:
10.1016/S0140-6736(05)63023-1
中图分类号
:
R5 [内科学];
学科分类号
:
1002 ;
100201 ;
摘要
:
[No abstract available]
引用
收藏
页码:1147 / 1147
页数:1
相关论文
共 5 条
[1]
MUTATIONS IN THE LAMININ ALPHA-2-CHAIN GENE (LAMA2) CAUSE MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY
HELBLINGLECLERC, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
HELBLINGLECLERC, A
ZHANG, X
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
ZHANG, X
TOPALOGLU, H
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
TOPALOGLU, H
CRUAUD, C
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
CRUAUD, C
TESSON, F
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
TESSON, F
WEISSENBACH, J
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
WEISSENBACH, J
TOME, FMS
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
TOME, FMS
SCHWARTZ, K
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
SCHWARTZ, K
FARDEAU, M
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
FARDEAU, M
论文数:
引用数:
h-index:
机构:
TRYGGVASON, K
GUICHENEY, P
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
GUICHENEY, P
[J].
NATURE GENETICS,
1995,
11
(02)
: 216
-
218
[2]
Nissinen M, 1996, AM J HUM GENET, V58, P1177
[3]
NOAM IS, 1997, J MED GENET, V34, P99
[4]
CLINICAL PHENOTYPE IN CONGENITAL MUSCULAR-DYSTROPHY - CORRELATION WITH EXPRESSION OF MEROSIN IN SKELETAL-MUSCLE
PHILPOT, J
论文数:
0
引用数:
0
h-index:
0
机构:
HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,NEUROMUSCULAR UNIT,LONDON W12 0NN,ENGLAND
PHILPOT, J
SEWRY, C
论文数:
0
引用数:
0
h-index:
0
机构:
HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,NEUROMUSCULAR UNIT,LONDON W12 0NN,ENGLAND
SEWRY, C
PENNOCK, J
论文数:
0
引用数:
0
h-index:
0
机构:
HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,NEUROMUSCULAR UNIT,LONDON W12 0NN,ENGLAND
PENNOCK, J
DUBOWITZ, V
论文数:
0
引用数:
0
h-index:
0
机构:
HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,NEUROMUSCULAR UNIT,LONDON W12 0NN,ENGLAND
DUBOWITZ, V
[J].
NEUROMUSCULAR DISORDERS,
1995,
5
(04)
: 301
-
305
[5]
TOME FMS, 1994, CR ACAD SCI III-VIE, V317, P351
←
1
→
共 5 条
[1]
MUTATIONS IN THE LAMININ ALPHA-2-CHAIN GENE (LAMA2) CAUSE MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY
HELBLINGLECLERC, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
HELBLINGLECLERC, A
ZHANG, X
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
ZHANG, X
TOPALOGLU, H
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
TOPALOGLU, H
CRUAUD, C
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
CRUAUD, C
TESSON, F
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
TESSON, F
WEISSENBACH, J
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
WEISSENBACH, J
TOME, FMS
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
TOME, FMS
SCHWARTZ, K
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
SCHWARTZ, K
FARDEAU, M
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
FARDEAU, M
论文数:
引用数:
h-index:
机构:
TRYGGVASON, K
GUICHENEY, P
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OULU,DEPT BIOCHEM,SF-90571 OULU,FINLAND
GUICHENEY, P
[J].
NATURE GENETICS,
1995,
11
(02)
: 216
-
218
[2]
Nissinen M, 1996, AM J HUM GENET, V58, P1177
[3]
NOAM IS, 1997, J MED GENET, V34, P99
[4]
CLINICAL PHENOTYPE IN CONGENITAL MUSCULAR-DYSTROPHY - CORRELATION WITH EXPRESSION OF MEROSIN IN SKELETAL-MUSCLE
PHILPOT, J
论文数:
0
引用数:
0
h-index:
0
机构:
HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,NEUROMUSCULAR UNIT,LONDON W12 0NN,ENGLAND
PHILPOT, J
SEWRY, C
论文数:
0
引用数:
0
h-index:
0
机构:
HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,NEUROMUSCULAR UNIT,LONDON W12 0NN,ENGLAND
SEWRY, C
PENNOCK, J
论文数:
0
引用数:
0
h-index:
0
机构:
HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,NEUROMUSCULAR UNIT,LONDON W12 0NN,ENGLAND
PENNOCK, J
DUBOWITZ, V
论文数:
0
引用数:
0
h-index:
0
机构:
HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,NEUROMUSCULAR UNIT,LONDON W12 0NN,ENGLAND
DUBOWITZ, V
[J].
NEUROMUSCULAR DISORDERS,
1995,
5
(04)
: 301
-
305
[5]
TOME FMS, 1994, CR ACAD SCI III-VIE, V317, P351
←
1
→