Identification of a new variant of TTR involved in familial amyloid cardiomyopathy (FAC) in Brazil: from the patient to the protein.

P Ferreira, C Andrade, R Santanna, N Varejão, S Ventura, F Palhano, M Cruz, D Foguel

Producció científica: Contribució a revista › Article › Recerca › Avaluat per experts

Idioma original	Anglès
Revista	Orphanet Journal of Rare Diseases
DOIs	https://doi.org/10.1186/1750-1172-10-s1-p55
Estat de la publicació	Publicada - 2015

Accés al document

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title = "Identification of a new variant of TTR involved in familial amyloid cardiomyopathy (FAC) in Brazil: from the patient to the protein.",

author = "P Ferreira and C Andrade and R Santanna and N Varej{\~a}o and S Ventura and F Palhano and M Cruz and D Foguel",

year = "2015",

doi = "10.1186/1750-1172-10-s1-p55",

language = "English",

journal = "Orphanet Journal of Rare Diseases",

issn = "1750-1172",

publisher = "BioMed Central Ltd.",

}

TY - JOUR

T1 - Identification of a new variant of TTR involved in familial amyloid cardiomyopathy (FAC) in Brazil: from the patient to the protein.

AU - Ferreira, P

AU - Andrade, C

AU - Santanna, R

AU - Varejão, N

AU - Ventura, S

AU - Palhano, F

AU - Cruz, M

AU - Foguel, D

PY - 2015

Y1 - 2015

UR - http://europepmc.org/abstract/PMC/PMC4641998

U2 - 10.1186/1750-1172-10-s1-p55

DO - 10.1186/1750-1172-10-s1-p55

M3 - Article

C2 - PMC4641998

SN - 1750-1172

JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

ER -