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Patient reported outcomes for phosphomannomutase 2 congenital disorder of glycosylation (PMM2-CDG): listening to what matters for the patients and health professionals
by
Pascoal, C
,
Ferreira, I
,
Teixeira, C
,
Almeida, E
,
Slade, A
,
Brasil, S
,
Francisco, R
,
Ligezka, A.N
,
Morava, E
,
Plotkin, H
,
Jaeken, J
,
Videira, P.A
,
Barros, L
,
dos Reis Ferreira, V
Published in
Orphanet journal of rare diseases
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Orphanet Journal Of Rare Diseases
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