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Search Results for - LEWANDOWSKY-LUTZ DISEASE

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ID
 
Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
 
EPIDERMODYSPLASIA VERRUCIFORMIS
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
EPIDERMODYSPLASIA VERRUCIFORMIS
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
EPIDERMODYSPLASIA VERRUCIFORMIS
 
Fibroblast
 
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE II, ALPHA-1; COL2A1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1
 
Fibroblast
 
Skin, Skin
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE II, ALPHA-1; COL2A1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE II, ALPHA-1; COL2A1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE II, ALPHA-1; COL2A1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE II, ALPHA-1; COL2A1
 
LCL
 
B-Lymphocyte
 
 
 
 
CENTRAL CORE DISEASE OF MUSCLE | RYANODINE RECEPTOR 1; RYR1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE II, ALPHA-1; COL2A1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE VI, ALPHA-1; COL6A1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE II, ALPHA-1; COL2A1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE II, ALPHA-1; COL2A1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE VI, ALPHA-1; COL6A1
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3 | PROTEIN O-MANNOSE BETA-1,2-N-ACETYLGLUCOSAMINYLTRANSFERASE; POMGNT1
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3 | PROTEIN O-MANNOSE BETA-1,2-N-ACETYLGLUCOSAMINYLTRANSFERASE; POMGNT1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE VI, ALPHA-2; COL6A2
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE II, ALPHA-1; COL2A1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE VI, ALPHA-2; COL6A2
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
MYOPATHY, CENTRONUCLEAR, 1; CNM1 | TITIN; TTN
 
Fibroblast
 
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
BETHLEM MYOPATHY
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MYOTUBULAR MYOPATHY 1; MTM1
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
DNA
 
Fibroblast
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4 (WALKER-WARBURG SYNDROME INCLUDED) | FUKUTIN; FKTN
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A | LAMININ, ALPHA-2; LAMA2
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A | LAMININ, ALPHA-2; LAMA2
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A | LAMININ, ALPHA-2; LAMA2
 
DNA
 
Fibroblast
 
 
 
 
MYOPATHY, CENTRONUCLEAR, 1; CNM1 | DYNAMIN 2; DNM2
 
LCL
 
B-Lymphocyte
 
 
 
 
PARKINSON DISEASE
 
DNA
 
Whole Blood

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