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. 2000 Oct;16(4):374.

doi: 10.1002/1098-1004(200010)16:4<374::AID-HUMU15>3.0.CO;2-4.

Identification of a novel missense mutation L329I in the episodic ataxia type 1 gene KCNA1--a challenging problem

M A Knight¹, E Storey, R J McKinlay Gardner, P Hand, S M Forrest

Affiliations

PMID: 11013453
DOI: 10.1002/1098-1004(200010)16:4<374::AID-HUMU15>3.0.CO;2-4

Identification of a novel missense mutation L329I in the episodic ataxia type 1 gene KCNA1--a challenging problem

M A Knight et al. Hum Mutat. 2000 Oct.

. 2000 Oct;16(4):374.

doi: 10.1002/1098-1004(200010)16:4<374::AID-HUMU15>3.0.CO;2-4.

Authors

M A Knight¹, E Storey, R J McKinlay Gardner, P Hand, S M Forrest

Affiliation

¹ Murdoch Childrens Research Institute, Royal Children's Hospital, Flemington Road, Parkville, Victoria, Australia.

PMID: 11013453
DOI: 10.1002/1098-1004(200010)16:4<374::AID-HUMU15>3.0.CO;2-4

No abstract available

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