Mutations in MAGEL2 and L1CAM are associated with congenital hypopituitarism and arthrogryposis

Authors :: Mehul T. Dattani
Jane A. Hurst
Louise Ocaka
Hywel Williams
Le Quesne Stabej P
Sanner Jrf
Martinez-guayo A
Wendy D Jones
Helen Spoudeas
Pratik Shah
Monica Arancibia
Carolina Loureiro
Louise C. Gregory
Source :: Yearbook of Paediatric Endocrinology.
Publication Year :: 2020
Publisher :: Bioscientifica, 2020.

Subjects :: Arthrogryposis
Pediatrics
medicine.medical_specialty
business.industry
medicine
Congenital hypopituitarism
medicine.symptom
medicine.disease
business

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