Molecular basis of genetic heterogeneity: role of the clinical neurologist.

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Dopa-responsive dystonia: recent advances and remaining issues to be addressed.The silver jubilee: Journal of Child Neurology turns 25.

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Molecular basis of genetic heterogeneity: role of the clinical neurologist.

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1998 nî lūn-bûn

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Molecular basis of genetic heterogeneity: role of the clinical neurologist.

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Molecular basis of genetic heterogeneity: role of the clinical neurologist.

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Molecular basis of genetic heterogeneity: role of the clinical neurologist.

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Molecular basis of genetic heterogeneity: role of the clinical neurologist.

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Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins

The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis

Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Crystal structure of the extracellular domain from P0, the major structural protein of peripheral nerve myelin

Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD)

Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

Spinal muscular atrophy

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Molecular basis of genetic heterogeneity: role of the clinical neurologist.

about

P2860

P2860

Molecular basis of genetic heterogeneity: role of the clinical neurologist.

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