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Search Results for - FAMILIAL INFANTILE MYASTHENIA

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ID
 
Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
 
MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
DNA
 
LCL
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1; PFIC1 | NEMALINE MYOPATHY 2, AUTOSOMAL RECESSIVE; NEM2
 
LCL
 
B-Lymphocyte
 
 
 
 
INCLUSION BODY MYOSITIS
 
LCL
 
B-Lymphocyte
 
 
 
 
CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2
 
Fibroblast
 
 
 
 
 
CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2
 
Fibroblast
 
 
 
 
 
CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2
 
Fibroblast
 
 
 
 
 
CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2
 
Fibroblast
 
 
 
 
 
SPINAL MUSCULAR ATROPHY I; SMA1
 
LCL
 
B-Lymphocyte
 
 
 
 
SPINAL MUSCULAR ATROPHY I; SMA1
 
DNA
 
LCL
 
 
 
 
CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2 | CLN2 GENE; CLN2
 
DNA
 
Fibroblast
 
 
 
 
CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2 | CLN2 GENE; CLN2
 
DNA
 
LCL
 
 
 
 
REFSUM DISEASE, INFANTILE FORM
 
Fibroblast
 
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
 
 
 
 
HYPOPHOSPHATASIA, INFANTILE | ALKALINE PHOSPHATASE, LIVER; ALPL
 
DNA
 
Fibroblast
 
 
 
 
REFSUM DISEASE, INFANTILE FORM
 
Fibroblast
 
 
 
 
 
REFSUM DISEASE, INFANTILE FORM
 
LCL
 
B-Lymphocyte
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
 
 
 
 
REFSUM DISEASE, INFANTILE FORM
 
LCL
 
B-Lymphocyte
 
 
 
 
REFSUM DISEASE, INFANTILE FORM
 
Fibroblast
 
 
 
 
 
CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2 | CLN2 GENE; CLN2
 
LCL
 
B-Lymphocyte
 
 
 
 
CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2 | CLN2 GENE; CLN2
 
Fibroblast
 
 
 
 
 
SPINAL MUSCULAR ATROPHY I; SMA1
 
DNA
 
LCL
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
LCL
 
B-Lymphocyte
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
 
 
 
 
LEIGH SYNDROME; LS
 
Fibroblast
 
 
 
 
 
SPINAL MUSCULAR ATROPHY I; SMA1
 
LCL
 
B-Lymphocyte
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
 
 
 
 
NEUROAXONAL DYSTROPHY, INFANTILE
 
DNA
 
Fibroblast
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
LCL
 
B-Lymphocyte
 
 
 
 
SPINAL MUSCULAR ATROPHY I; SMA1
 
LCL
 
B-Lymphocyte
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
 
 
 
 
LACTIC ACIDOSIS, CONGENITAL INFANTILE
 
Fibroblast
 
 
 
 
 
NEUROAXONAL DYSTROPHY, INFANTILE
 
Fibroblast
 
 
 
 
 
SPINAL MUSCULAR ATROPHY I; SMA1
 
LCL
 
B-Lymphocyte
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Amniotic fluid-derived cell line
 
Amniotic fluid
 
 
 
 
NEUROAXONAL DYSTROPHY, INFANTILE
 
Fibroblast
 
 
 
 
 
LACTIC ACIDOSIS, CONGENITAL INFANTILE
 
Fibroblast
 
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
DNA
 
LCL

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