See also "P Leane"
adrenoleukodystrophy fibroblasts FNDC5 Infantile Refsum's disease PEX1 PEX6 PHEX PSMC2 skin SLC14A2 Zellweger's syndrome
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1 literature result
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Novel PEX1 coding mutations and 5' UTR regulatory polymorphisms.
Zellweger syndrome and its milder variants--neonatal adrenoleukodystrophy and infantile Refsum disease--comprise a clinical continuum of diseases refe…
Authors: Megan A Maxwell, Pamela B Leane, Barbara C Paton, Denis I Crane
Source: Human mutation. 2005 Sep
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