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Novel mutations seen in rapid, fatal case of early onset LAL deficiency (Wolman disease)
by
Gomez-Najera, Mariana
,
Barajas-Medina, Hilario
,
Gallegos-Rivas, Mayra Celina
,
Mendez-Sashida, Pedro
,
Simonds, Amy
,
Tripuraneni, Radhika
,
Valles-Ayoub, Yadira
,
Eroglu, Yasemen
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Molecular genetics and metabolism
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