New clinical forms of hereditary apoA-I amyloidosis entail both glomerular and retinal amyloidosis.
Colombat M, Aldigier JC, Rothschild PR, Javaugue V, Desport E, Frouget T, Goujon JM, Rioux-Leclercq N, Quellard N, Rerolle JP, Paraf F, Beugnet C, Tiple A, Durrbach A, Samuel D, Brézin A, Bridoux F, Valleix S.
Colombat M, et al. Among authors: beugnet c.
Kidney Int. 2020 Jul;98(1):195-208. doi: 10.1016/j.kint.2020.03.033. Epub 2020 Apr 23.
Kidney Int. 2020.
PMID: 32571483
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