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Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis.

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Title: Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis.
Authors: Kaplan JM; Renal and Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA., Kim SH, North KN, Rennke H, Correia LA, Tong HQ, Mathis BJ, Rodríguez-Pérez JC, Allen PG, Beggs AH, Pollak MR
Source: Nature genetics [Nat Genet] 2000 Mar; Vol. 24 (3), pp. 251-6.
Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
Journal Info: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print Cited Medium: Print ISSN: 1061-4036 (Print) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis.
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  Data: <searchLink fieldCode="JN" term="%229216904%22">Nature genetics</searchLink> [Nat Genet] 2000 Mar; Vol. 24 (3), pp. 251-6.
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              Text: 2000 Mar
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