Homozygotie And NotMiriam Y. Neufeld

List of bibliographic references

Number of relevant bibliographic references: 3.

Ident.	Authors (with country if any)	Title
002F17	G. A. Nicholson [Australie] ; C. Magdelaine [France] ; D. Zhu [Australie] ; S. Grew [Australie] ; M. M. Ryan [Australie] ; F. Sturtz [France] ; J.-M. Vallat [France] ; R. A. Ouvrier [Australie]	Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations
004F49	Ferdinando Squitieri [Italie] ; Cinzia Gellera [Italie] ; Milena Cannella [Italie] ; Caterina Mariotti [Italie] ; Giuliana Cislaghi [Italie] ; David C. Rubinsztein [Royaume-Uni] ; Elisabeth W. Almqvist [Canada] ; David Turner [Australie] ; Anne-Catherine Bachoud-Levi [France] ; Sheila A. Simpson [Royaume-Uni] ; Martin Delatycki [Australie] ; Vittorio Maglione [Italie] ; Michael R. Hayden [Canada] ; Stefano Di Donato [Italie]	Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course
005911	Stephanie Portrat [France] ; Paolo Mulatero [Italie] ; Kathleen M. Curnow [Australie] ; Jean-Louis Chaussain [France] ; Yves Morel [France] ; Leigh Pascoe [France]	Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11β-hydroxylase) and CYP11B2 (aldosterone synthase) cause steroid 11β-hydroxylase deficiency and congenital adrenal hyperplasia

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