Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aalpha chain gene. (Q53612268)
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Language | Label | Description | Also known as |
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English | Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aalpha chain gene. |
scientific article |
Statements
Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aalpha chain gene. (English)
Hee Gyung Kang
Alison Bybee
Il Soo Ha
Moon Soo Park
Janet A Gilbertson
Hae Il Cheong
Yong Choi
Philip N Hawkins
1 November 2005
68
5
1994-1998