神经节苷脂病
先证者
表型
分子遗传学
医学遗传学
生物
遗传学
医学
生物信息学
疾病
突变
基因
内科学
作者
Abdellah Tebani,Bénédicte Sudrié‐Arnaud,Ivana Dabaj,Stéphanie Torre,Domitille Laur,Sarah Snanoudj,Bénédicte Héron,Thierry Levade,Catherine Caillaud,Sabrina Vergnaud,Pascale Saugier-Véber,Sophie Coutant,Hélène Dranguet,Roseline Froissart,Majed Al Khouri,Yves Alembik,Julien Baruteau,Jean‐Baptiste Arnoux,Anaïs Brassier,Anne‐Claire Bréhin
标识
DOI:10.1136/jmedgenet-2020-107510
摘要
This study reports one of the largest series of b-GAL deficiency with an integrative patient stratification combining molecular and clinical features. This work contributes to expand the community knowledge regarding the molecular and clinical landscapes of b-GAL deficiency for a better patient management.
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