X-chromosome inactivation in female patients with Fabry disease-Reference-Cited by-同舟云学术

X-chromosome inactivation in female patients with Fabry disease

Author:

Echevarria L.¹²,Benistan K.²,Toussaint A.³,Dubourg O.⁴,Hagege A.A.⁵,Eladari D.⁶,Jabbour F.²,Beldjord C.³,De Mazancourt P.⁷,Germain D.P.¹²⁷

Affiliation:

1. Division of Medical Genetics; University of Versailles; Montigny France

2. Assistance Publique - Hôpitaux de Paris (AP-HP); Referral Center for Fabry Disease and Inherited Disorders of Connective Tissue; Garches France

3. Laboratory of Biochemistry and Molecular Biology; University Paris V Descartes; Paris France

4. Department of Cardiology; University of Versailles; Boulogne France

5. Department of Cardiology, HEGP (APHP); Paris France

6. Department of Physiology, HEGP (APHP); University Paris V Descartes; Paris France

7. UFR des sciences de la santé; University of Versailles; Montigny France

Funder

Plan National Maladies Rares (French Ministry of Heath)

Genzyme

Shrine

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference63 articles.

1. Fabry disease;Germain;Orphanet J Rare Dis,2010

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