(Q38337830)

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Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene

scientific article published in December 1990

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2 September 2017

Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene (English)

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2 September 2017

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2

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Albert de la Chapelle

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4

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de la Chapelle A

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Maury CP

1

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Tolvanen R

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3

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2 September 2017

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English

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1 December 1990

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276

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75-77

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1-2

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2 September 2017

Plasma and cytoplasmic gelsolins are encoded by a single gene and contain a duplicated actin-binding domain

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21 January 2018

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

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21 January 2018

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

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21 January 2018

Human gene for torsion dystonia located on chromosome 9q32-q34.

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21 January 2018

Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy

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21 January 2018

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DOI

10.1016/0014-5793(90)80510-P

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2 September 2017

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2 September 2017

(Q38337830)

Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene

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