Complex p.T88N/W130R mutation in the lysozyme gene leading to hereditary lysozyme amyloidosis with biopsy-proven cardiac involvement

Brett W. Sperry, Angela Dispenzieri, Asad Ikram, Martha Grogan, Jason D. Theis, Nelson Leung, W Edward Jr. Highsmith, Joseph Maleszewski, Mazen Hanna

Research output: Contribution to journalArticle

1 Citation (Scopus)
Original languageEnglish (US)
Pages (from-to)1-2
Number of pages2
JournalAmyloid
DOIs
StateAccepted/In press - Jan 16 2017

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Familial Amyloidosis
Muramidase
Biopsy
Mutation
Genes

ASJC Scopus subject areas

  • Internal Medicine

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Complex p.T88N/W130R mutation in the lysozyme gene leading to hereditary lysozyme amyloidosis with biopsy-proven cardiac involvement. / Sperry, Brett W.; Dispenzieri, Angela; Ikram, Asad; Grogan, Martha; Theis, Jason D.; Leung, Nelson; Highsmith, W Edward Jr.; Maleszewski, Joseph; Hanna, Mazen.

In: Amyloid, 16.01.2017, p. 1-2.

Research output: Contribution to journalArticle

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AU - Grogan, Martha

AU - Theis, Jason D.

AU - Leung, Nelson

AU - Highsmith, W Edward Jr.

AU - Maleszewski, Joseph

AU - Hanna, Mazen

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