FMR1 premutation with Prader-Willi phenotype and fragile X-associated tremor/ataxia syndrome-Reference-Cited by-同舟云学术

FMR1 premutation with Prader-Willi phenotype and fragile X-associated tremor/ataxia syndrome

Author:

Martínez-Cerdeño Verónica¹²³^ORCID,Lechpammer Mirna¹,Noctor Stephen³⁴,Ariza Jeanelle¹²,Hagerman Paul⁵,Hagerman Randi³⁶

Affiliation:

1. Department of Pathology and Laboratory Medicine; UC Davis Medical Center; Sacramento CA USA

2. Institute for Pediatric Regenerative Medicine and Shriners Hospitals for Children Northern California; Sacramento CA USA

3. MIND Institute; UC Davis Medical Center; Sacramento CA USA

4. Department of Psychiatry and Behavioral Sciences; UC Davis Medical Center; Sacramento CA USA

5. Department of Biochemistry and Molecular Medicine; UC Davis Medical Center; Sacramento CA USA

6. Department of Pediatrics; UC Davis Medical Center; Sacramento CA USA

Funder

National Institutes of Health

Shiners Hospitals

Publisher

Wiley

Subject

General Medicine

Link

Reference18 articles.

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