A new family with hereditary lysozyme amyloidosis with gastritis and inflammatory bowel disease as prevailing symptoms.
about
Lysozyme Mutants Accumulate in Cells while Associated at their N-terminal Alpha-domain with the Endoplasmic Reticulum Chaperone GRP78/BiP.Hereditary Lysozyme Amyloidosis Variant p.Leu102Ser Associates with Unique Phenotype.Hereditary lysozyme amyloidosis with sicca syndrome, digestive, arterial, and tracheobronchial involvement: case-based review.The extreme hyper-reactivity of Cys94 in lysozyme avoids its amorphous aggregation
P2860
A new family with hereditary lysozyme amyloidosis with gastritis and inflammatory bowel disease as prevailing symptoms.
description
2014 nî lūn-bûn
@nan
2014 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
A new family with hereditary l ...... isease as prevailing symptoms.
@ast
A new family with hereditary l ...... isease as prevailing symptoms.
@en
type
label
A new family with hereditary l ...... isease as prevailing symptoms.
@ast
A new family with hereditary l ...... isease as prevailing symptoms.
@en
prefLabel
A new family with hereditary l ...... isease as prevailing symptoms.
@ast
A new family with hereditary l ...... isease as prevailing symptoms.
@en
P2093
P2860
P356
P1433
P1476
A new family with hereditary l ...... isease as prevailing symptoms.
@en
P2093
Aurélie Grados
Brigitte Granel
Emmanuelle Bernit
Estelle Jean
Gilles Grateau
Jean-Robert Harlé
Laurent Daniel
Laurent Heyries
Lucas Benarous
Mikael Ebbo
P2860
P2888
P356
10.1186/1471-230X-14-159
P577
2014-09-13T00:00:00Z
P5875
P6179
1044214991